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: 25 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WXA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.623 |
DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.698 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.621 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.570 |
DOC_CYCLIN_RxL_1 | 115 | 125 | PF00134 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.693 |
DOC_MAPK_FxFP_2 | 202 | 205 | PF00069 | 0.557 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.512 |
DOC_PP4_MxPP_1 | 39 | 42 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.510 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.565 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 402 | 408 | PF00928 | 0.389 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.683 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.337 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.655 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.569 |
LIG_Integrin_RGDW_4 | 306 | 309 | PF00362 | 0.385 |
LIG_LIR_Apic_2 | 201 | 205 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 319 | 323 | PF02991 | 0.389 |
LIG_LIR_Apic_2 | 413 | 417 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 253 | 260 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.368 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.418 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.434 |
LIG_SH2_GRB2like | 430 | 433 | PF00017 | 0.383 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.398 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.383 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.482 |
LIG_SH2_STAT6 | 198 | 202 | PF00017 | 0.553 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.596 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.615 |
LIG_SUMO_SIM_par_1 | 174 | 182 | PF11976 | 0.570 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.549 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.520 |
MOD_CDK_SPK_2 | 49 | 54 | PF00069 | 0.545 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.694 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.567 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.434 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.525 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.573 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.528 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.325 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.669 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.391 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.434 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.373 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.746 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.699 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.635 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.535 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.693 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.374 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.388 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.700 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.428 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.695 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.440 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.552 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.597 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.489 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.474 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.542 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.424 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.583 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.563 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.325 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.504 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.454 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.286 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.773 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.503 |
MOD_PKB_1 | 188 | 196 | PF00069 | 0.642 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.563 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.695 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.481 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.459 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.730 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.343 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.342 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.426 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.528 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.538 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.773 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.653 |
MOD_SUMO_for_1 | 326 | 329 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 263 | 269 | PF00179 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.694 |
TRG_DiLeu_BaLyEn_6 | 519 | 524 | PF01217 | 0.580 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.434 |
TRG_LysEnd_GGAAcLL_1 | 520 | 526 | PF00790 | 0.584 |
TRG_NES_CRM1_1 | 175 | 189 | PF08389 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIF6 | Leptomonas seymouri | 68% | 92% |
A0A1X0NTG8 | Trypanosomatidae | 44% | 100% |
A0A1X0P961 | Trypanosomatidae | 29% | 76% |
A0A3R7NAK8 | Trypanosoma rangeli | 45% | 100% |
A0A3S7X3U7 | Leishmania donovani | 36% | 100% |
A4HCH7 | Leishmania braziliensis | 87% | 100% |
A4HIR9 | Leishmania braziliensis | 36% | 100% |
A4HZZ9 | Leishmania infantum | 100% | 100% |
A4I615 | Leishmania infantum | 36% | 100% |
C9ZSQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A328 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 76% |
E9AVX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B1A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4Q6V8 | Leishmania major | 36% | 100% |
Q4QBK7 | Leishmania major | 96% | 100% |