Structure of PDB 7ni5 Chain A Binding Site BS02

Receptor Information
>7ni5 Chain A (length=2791) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
LVLNDLLICCRQLEHDRATERKKEVEKFKRLIRDPETIKHLDRHSDSKQG
KYLNWDAVFRFLQKYIQKETECLRIASTQASRQKKMQEISSLVKYFIKCA
NRRAPRLKCQELLNYIMDTVKDSSNGAIYGADCSNILLKDILSVRKYWCE
ISQQQWLELFSVYFRLYLKPSQDVHRVLVARIIHAVTKGCCSQTDGLNSK
FLDFFSKAIQCARQEKSSSGLNHILAALTIFLKTLAVNFRIRVCELGDEI
LPTLLYIWTQHRLNDSLKEVIIELFQLQIYIHHPKGAKTQEKGAYESTKW
RSILYNLYDLLVNEISHIGSRGKYSSGFRNIAVKENLIELMADICHQVFI
ELGWEVIKDHLQKSQNDFDLVPWLQIATQLISKYPASLPNCELSPLLMIL
SQLLPQQRHGERTPYVLRCLTEVALCQDKRSNLESSQKSDLLKLWNKIWC
ITFRGISSEQIQAENFGLLGAIIQGSLVEVDREFWKLFTGSACRPSCPAV
CCLTLALTTSIVPGTFSLKESIMKWLLFYQEVPPILHSNFPHLVLEKILV
SLTMKNCKAAMNFFQSVPECEHHQKDKEELSFSEVEELFLQTTFDKMDFL
TSSIGFSVHQNLKESLDRCLLGLSEQLLNNYSSEITNSETLVRCSRLLVG
VLGCYCYMGVIAEEEAYKSELFQKAKSLMQCAGESITLFKNKTNEEFRIG
SLRNMMQLCTRCLSNCTKKSPNKIASGFFLRLLTSKLMNDIADICKSLAS
FIKKIGAINPLAEEYLSKQDLLFLDMLKFLCLCVTTAQTNTVSFRAADIR
RKLLMLIDSSTLEPTKSLHLHMYLMLLKELPGEEYPLPMEDVLELLKPLS
NVCSLYRRDQDVCKTILNHVLHVVKNLGQSNMDSENTRDAQGQFLTVIGA
FWHLTKERKYIFSVRMALVNCLKTLLEADPYSKWAILNVMGKDFPVNEVF
TQFLADNHHQVRMLAAESINRLFQDTLLKALPLKLQQTAFENAYLKAQEG
MREMSHSAENPETLDEIYNRKSVLLTLIAVVLSCSPICEKQALFALCKSV
KENGLEPHLVKKVLEKVSETFGYRRLEDFMASHLDYLVLEWLNLQDTEYN
LSSFPFILLNYTNIEDFYRSCYKVLIPHLVIRSHFDEVKSIANQIQEDWK
SLLTDCFPKILVNILPYFAYEGTRDSGMAQQRETATKVYDMLKSENLLGK
QIDHLFISNLPEIVVELLMTLHEPDLDPAPNPPHFPSHVIKATFAYISNC
ILEILSKSPDSYQKILLAICEQAAETNNVYKKHRILKIYHLFVSLLLKDI
KSGLGGAWAFVLRDVIYTLIHYINQRPSCIMDVSLRSFSLCCDLLSQVCQ
TAVTYCKDALENHLHVIVGTLIPLVYEQVEVQKQVLDLLKYLVIDNKDNE
NLYITIKLLDPFPDHVVFKDLRITQQKIKYSRGPFSLLEEINHFLSVSVY
DALPLTRLEGLKDLRRQLELHKDQMVDIMRASQDNPQDGIMVKLVVNLLQ
LSKMAINHTGEKEVLEAVGSCLGEVGPIDFSTIAIQHSKDASYTKALKLF
EDKELQWTFIMLTYLNNTLVEDCVKVRSAAVTCLKNILATKTGHSFWEIY
KMTTDPMLAYLQPFRTSRKKFLEVPRFDKENPFEGLDDINLWIPLSENHD
IWIKTLTCAFLDSGGTKCEILQLLKPMCEVKTDFCQTVLPYLIHDILLQD
TNESWRNLLSTHVQGFFTSCLRHHFFRCCLDKKSQRTMLAVVDYMRRQKR
PSSGTIFNDAFWLDLNYLEVAKVAQSCAAHFTALLYAEIYADKKSMDDQE
KISSLSEKSKEETGISLQDLLLEIYRSIGEPDSLYGCGGGKMLQPITRLR
TYEHEAMWGKALVTYDLETAIPSSTRQAGIIQALQNLGLCHILSVYLKGL
DYENKDWCPELEELHYQAAWRNMQWDHCGTSYHESLYNALQSLRDREFST
FYESLKYARVKEVEEMCKRSLESVYSLYPTLSRLQAIGELESIGELFSRS
VTHRQLSEVYIKWQKHSQLLKDSDFSFQEPIMALRTVILEILMEKEMDNS
QRECIKDILTKHLVELSILARTFKNTQLPERAIFQIKQYNSVSCGVSEWQ
LEEAQVFWAKKEQSLALSILKQMIKKLDASCAANNPSLKLTYTECLRVCG
NWLAETCLENPAVIMQTYLEKAVEVASDELRNGKMKAFLSLARFSDTQYQ
RIENYMKSSEFENKQALLKRQRELELDELALRALKEDRKRFLCKAVENYI
NCLLSGEEHDMWVFRLCSLWLENSGVSEVNGMMKRDGMKIPTYKFLPLMY
QLAARMGTKMMGGLGFHEVLNNLISRISMDHPHHTLFIILALANANRDEF
LTKSQLDEDRTEAANRIICTIRSRRPQMVRSVEALCDAYIILANLDATQW
KTQRKGINIPADQPITKLKNLEDVVVPTMEIKVDHTGEYGNLVTIQSFKA
EFRLAGGVNLPKIIDCVGSDGKERRQLVKGRDDLRQDAVMQQVFQMCNTL
LQRNTETRKRKLTICTYKVVPLSQRSGVLEWCTGTVPIGEFLVNNEDGAH
KRYRPNDFSAFQCQKKMMEVQKKSFEEKYEVFMDVCQNFQPVFRYFCMEK
FLDPAIWFEKRLAYTRSVATSSIVGYILGLGDRHVQNILINEQSAELVHI
DLGVAFEQGKILPTPETVPFRLTRDIVDGMGITGVEGVFRRCCEKTMEVM
RNSQETLLTIVEVLLYDPLFDWTMNPLKALYLQQQSFNKVAERVLMRLQE
KLKGVEEGTVLSVGGQVNLLIQQAIDPKNLSRLFPGWKAWV
Ligand information
Ligand IDZN
InChIInChI=1S/Zn/q+2
InChIKeyPTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
FormulaZn
NameZINC ION
ChEMBLCHEMBL1236970
DrugBankDB14532
ZINC
PDB chain7ni5 Chain A Residue 3102 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB7ni5 Molecular basis of human ATM kinase inhibition.
Resolution2.78 Å
Binding residue
(original residue number in PDB)
H1876 H1895 C1900
Binding residue
(residue number reindexed from 1)
H1723 H1724 C1729
Annotation score1
Enzymatic activity
Enzyme Commision number 2.7.11.1: non-specific serine/threonine protein kinase.
Gene Ontology
Molecular Function
GO:0003677 DNA binding
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0004677 DNA-dependent protein kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016301 kinase activity
GO:0016303 1-phosphatidylinositol-3-kinase activity
GO:0035979 histone H2AXS139 kinase activity
GO:0042802 identical protein binding
GO:0044024 histone H2AS1 kinase activity
GO:0044877 protein-containing complex binding
GO:0106310 protein serine kinase activity
Biological Process
GO:0000077 DNA damage checkpoint signaling
GO:0000425 pexophagy
GO:0000723 telomere maintenance
GO:0000724 double-strand break repair via homologous recombination
GO:0000729 DNA double-strand break processing
GO:0001541 ovarian follicle development
GO:0001666 response to hypoxia
GO:0001756 somitogenesis
GO:0002331 pre-B cell allelic exclusion
GO:0002376 immune system process
GO:0006281 DNA repair
GO:0006302 double-strand break repair
GO:0006303 double-strand break repair via nonhomologous end joining
GO:0006338 chromatin remodeling
GO:0006468 protein phosphorylation
GO:0006974 DNA damage response
GO:0006977 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
GO:0007094 mitotic spindle assembly checkpoint signaling
GO:0007095 mitotic G2 DNA damage checkpoint signaling
GO:0007131 reciprocal meiotic recombination
GO:0007140 male meiotic nuclear division
GO:0007143 female meiotic nuclear division
GO:0007165 signal transduction
GO:0007292 female gamete generation
GO:0007420 brain development
GO:0007507 heart development
GO:0008340 determination of adult lifespan
GO:0008585 female gonad development
GO:0008630 intrinsic apoptotic signaling pathway in response to DNA damage
GO:0009791 post-embryonic development
GO:0010212 response to ionizing radiation
GO:0010506 regulation of autophagy
GO:0010628 positive regulation of gene expression
GO:0016310 phosphorylation
GO:0018105 peptidyl-serine phosphorylation
GO:0030335 positive regulation of cell migration
GO:0030889 negative regulation of B cell proliferation
GO:0032210 regulation of telomere maintenance via telomerase
GO:0032212 positive regulation of telomere maintenance via telomerase
GO:0033151 V(D)J recombination
GO:0033554 cellular response to stress
GO:0034614 cellular response to reactive oxygen species
GO:0035264 multicellular organism growth
GO:0036092 phosphatidylinositol-3-phosphate biosynthetic process
GO:0036289 peptidyl-serine autophosphorylation
GO:0042159 lipoprotein catabolic process
GO:0042770 signal transduction in response to DNA damage
GO:0042981 regulation of apoptotic process
GO:0043065 positive regulation of apoptotic process
GO:0043517 positive regulation of DNA damage response, signal transduction by p53 class mediator
GO:0043525 positive regulation of neuron apoptotic process
GO:0045141 meiotic telomere clustering
GO:0045785 positive regulation of cell adhesion
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0046777 protein autophosphorylation
GO:0048538 thymus development
GO:0048599 oocyte development
GO:0051402 neuron apoptotic process
GO:0051726 regulation of cell cycle
GO:0070192 chromosome organization involved in meiotic cell cycle
GO:0071044 histone mRNA catabolic process
GO:0071300 cellular response to retinoic acid
GO:0071479 cellular response to ionizing radiation
GO:0071480 cellular response to gamma radiation
GO:0071481 cellular response to X-ray
GO:0071500 cellular response to nitrosative stress
GO:0080090 regulation of primary metabolic process
GO:0080135 regulation of cellular response to stress
GO:0090398 cellular senescence
GO:0090399 replicative senescence
GO:0097694 establishment of RNA localization to telomere
GO:0097695 establishment of protein-containing complex localization to telomere
GO:1900034 regulation of cellular response to heat
GO:1901796 regulation of signal transduction by p53 class mediator
GO:1903626 positive regulation of DNA catabolic process
GO:1903978 regulation of microglial cell activation
GO:1904262 negative regulation of TORC1 signaling
GO:1904354 negative regulation of telomere capping
GO:1904358 positive regulation of telomere maintenance via telomere lengthening
GO:1904884 positive regulation of telomerase catalytic core complex assembly
GO:2000785 regulation of autophagosome assembly
Cellular Component
GO:0000781 chromosome, telomeric region
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005777 peroxisome
GO:0005782 peroxisomal matrix
GO:0005813 centrosome
GO:0005819 spindle
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0031410 cytoplasmic vesicle
GO:0035861 site of double-strand break
GO:0043231 intracellular membrane-bounded organelle
GO:0098850 extrinsic component of synaptic vesicle membrane
GO:1990391 DNA repair complex

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:7ni5, PDBe:7ni5, PDBj:7ni5
PDBsum7ni5
PubMed34556870
UniProtQ13315|ATM_HUMAN Serine-protein kinase ATM (Gene Name=ATM)

[Back to BioLiP]