Browse>2CV5:D
Detailed Infomation
PDBChain | PTM Type | PTM Position in PDBChain |
UniProt ACC | PTM Position | UniProtID | Organism |
---|---|---|---|---|---|---|
2CV5:D | Acetylation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
2CV5:D | Ubiquitylation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
2CV5:D | 2-hydroxyisobutyrylation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
2CV5:D | Glycation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
2CV5:D | Malonylation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
2CV5:D | Succinylation_K | 117 | O60814 | 117 | H2B1K_HUMAN | Homo sapiens (Human) |
Mutations affecting PTM Sites
gene | refseq | mutation Position |
mutation Alt |
mutation Summary |
site Position | site Residue | uniprot ACC | uniprot ID |
---|---|---|---|---|---|---|---|---|
HIST1H2BK | NM_001312653 | 123 | A | STAD | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 114 | D | COAD | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_001312653 | 114 | D | COAD | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 110 | Y | DLBC | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 114 | K | HNSC | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 123 | A | STAD | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 114 | Q | HNSC | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_001312653 | 110 | Y | DLBC | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_001312653 | 114 | K | HNSC | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_001312653 | 114 | Q | HNSC | 117 | K | O60814 | H2B1K_HUMAN |
gene | refseq | mutation Position |
mutation Alt |
mutation Summary |
site Position | site Residue | uniprot ACC | uniprot ID |
---|---|---|---|---|---|---|---|---|
HIST1H2BK | NM_080593 | 124 | C | 0.000199681 | 117 | K | O60814 | H2B1K_HUMAN |
HIST1H2BK | NM_080593 | 112 | M | 0.000199681 | 117 | K | O60814 | H2B1K_HUMAN |
Protein Feature View
Sequence Alignment
Disorder picture
Sequence view
