Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000813 | ESCRT I complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0036452 | ESCRT complex | 2 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
Related structures:
AlphaFold database: Q4Q8L4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.390 |
DEG_ODPH_VHL_1 | 39 | 51 | PF01847 | 0.402 |
DOC_CKS1_1 | 216 | 221 | PF01111 | 0.458 |
DOC_CKS1_1 | 74 | 79 | PF01111 | 0.628 |
DOC_CYCLIN_RxL_1 | 208 | 218 | PF00134 | 0.309 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 263 | 267 | PF12436 | 0.467 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 5 | 12 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.629 |
LIG_CtBP_PxDLS_1 | 117 | 121 | PF00389 | 0.651 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.658 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.637 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.652 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.309 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.575 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.436 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.535 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.585 |
LIG_LIR_Gen_1 | 48 | 58 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.483 |
LIG_PCNA_yPIPBox_3 | 151 | 163 | PF02747 | 0.542 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 262 | 265 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.612 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.554 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.452 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.476 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.481 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.562 |
LIG_SH3_CIN85_PxpxPR_1 | 58 | 63 | PF14604 | 0.564 |
LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.550 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.673 |
LIG_UBA3_1 | 271 | 275 | PF00899 | 0.465 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.605 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.595 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.452 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.593 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.452 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.309 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.612 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.483 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.539 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.598 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.513 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.682 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.598 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.645 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.580 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.481 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.541 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.642 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.515 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.403 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.505 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.547 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.515 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.632 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.522 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.616 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.519 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.473 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.616 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.649 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.549 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.476 |
MOD_Plk_2-3 | 182 | 188 | PF00069 | 0.530 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.564 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.500 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.510 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.565 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.416 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.560 |
TRG_DiLeu_BaEn_1 | 130 | 135 | PF01217 | 0.688 |
TRG_DiLeu_BaEn_1 | 208 | 213 | PF01217 | 0.464 |
TRG_DiLeu_LyEn_5 | 130 | 135 | PF01217 | 0.688 |
TRG_DiLeu_LyEn_5 | 208 | 213 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.479 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q4 | Leptomonas seymouri | 77% | 100% |
A0A0S4JBQ7 | Bodo saltans | 31% | 100% |
A0A1X0NYI9 | Trypanosomatidae | 41% | 100% |
A0A3S7X186 | Leishmania donovani | 96% | 100% |
A0A422P1P4 | Trypanosoma rangeli | 40% | 100% |
A4HG97 | Leishmania braziliensis | 85% | 100% |
A4I3D0 | Leishmania infantum | 95% | 100% |
D0A814 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AZL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5DH66 | Trypanosoma cruzi | 42% | 93% |