Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HYS2
Term | Name | Level | Count |
---|---|---|---|
GO:0000070 | mitotic sister chromatid segregation | 4 | 10 |
GO:0000819 | sister chromatid segregation | 4 | 10 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007059 | chromosome segregation | 2 | 11 |
GO:0007062 | sister chromatid cohesion | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022402 | cell cycle process | 2 | 11 |
GO:0022414 | reproductive process | 1 | 11 |
GO:0045132 | meiotic chromosome segregation | 3 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0098813 | nuclear chromosome segregation | 3 | 11 |
GO:1903046 | meiotic cell cycle process | 2 | 11 |
GO:1903047 | mitotic cell cycle process | 3 | 11 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016407 | acetyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016746 | acyltransferase activity | 3 | 11 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
GO:0008080 | N-acetyltransferase activity | 6 | 1 |
GO:0016410 | N-acyltransferase activity | 5 | 1 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 1 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.651 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.621 |
CLV_PCSK_PC7_1 | 70 | 76 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.569 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 243 | 249 | PF00149 | 0.550 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.467 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 97 | 103 | PF00244 | 0.530 |
LIG_Clathr_ClatBox_1 | 217 | 221 | PF01394 | 0.497 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.386 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.344 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.422 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.707 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.605 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.473 |
LIG_REV1ctd_RIR_1 | 64 | 74 | PF16727 | 0.523 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 260 | 264 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.501 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.421 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.476 |
LIG_SUMO_SIM_par_1 | 211 | 221 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.456 |
LIG_TYR_ITIM | 258 | 263 | PF00017 | 0.544 |
LIG_TYR_ITIM | 270 | 275 | PF00017 | 0.561 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.505 |
MOD_CDK_SPxxK_3 | 247 | 254 | PF00069 | 0.552 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.486 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.303 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.653 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.649 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.540 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.543 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.493 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.331 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.654 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.492 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.491 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.436 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.365 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.633 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.678 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.237 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.469 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.600 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.674 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.725 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.517 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.663 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.674 |
MOD_LATS_1 | 96 | 102 | PF00433 | 0.490 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.750 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.446 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.567 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.494 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.546 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.679 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.516 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.427 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.622 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.655 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.584 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.472 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.467 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.517 |
TRG_NLS_MonoCore_2 | 96 | 101 | PF00514 | 0.495 |
TRG_NLS_MonoExtC_3 | 72 | 77 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 97 | 102 | PF00514 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4N8 | Leptomonas seymouri | 37% | 100% |
A0A1X0NWH5 | Trypanosomatidae | 34% | 92% |
A0A3S7WVV5 | Leishmania donovani | 100% | 100% |
A0A422MWP0 | Trypanosoma rangeli | 35% | 99% |
C9ZIA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AI91 | Leishmania braziliensis | 70% | 100% |
E9AUH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QD07 | Leishmania major | 87% | 100% |
V5DS57 | Trypanosoma cruzi | 32% | 100% |