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: 10 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0101031 | protein folding chaperone complex | 3 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AZE8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.504 |
CLV_PCSK_FUR_1 | 305 | 309 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.584 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.290 |
DEG_APCC_DBOX_1 | 184 | 192 | PF00400 | 0.269 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.558 |
DEG_SPOP_SBC_1 | 222 | 226 | PF00917 | 0.532 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.721 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.766 |
DOC_CKS1_1 | 379 | 384 | PF01111 | 0.517 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.519 |
DOC_MAPK_gen_1 | 304 | 314 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.248 |
DOC_MAPK_MEF2A_6 | 307 | 316 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 454 | 462 | PF00069 | 0.464 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.381 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.508 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.458 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.469 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.456 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.408 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.706 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.480 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.499 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.655 |
LIG_LIR_Gen_1 | 384 | 392 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.435 |
LIG_PCNA_PIPBox_1 | 398 | 407 | PF02747 | 0.534 |
LIG_Pex14_2 | 388 | 392 | PF04695 | 0.448 |
LIG_SH2_GRB2like | 134 | 137 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 164 | 168 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 405 | 408 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.448 |
LIG_SH3_1 | 478 | 484 | PF00018 | 0.573 |
LIG_SH3_2 | 481 | 486 | PF14604 | 0.589 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.593 |
LIG_SUMO_SIM_anti_2 | 310 | 320 | PF11976 | 0.654 |
LIG_SUMO_SIM_anti_2 | 472 | 479 | PF11976 | 0.447 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.528 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.648 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.604 |
LIG_UBA3_1 | 426 | 435 | PF00899 | 0.436 |
LIG_WRC_WIRS_1 | 434 | 439 | PF05994 | 0.534 |
MOD_CDK_SPK_2 | 378 | 383 | PF00069 | 0.470 |
MOD_CDK_SPxK_1 | 480 | 486 | PF00069 | 0.540 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.469 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.652 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.661 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.643 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.652 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.462 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.501 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.622 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.446 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.575 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.284 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.484 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.536 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.539 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.356 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.415 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.654 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.710 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.719 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.528 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.592 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.680 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.567 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.645 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.596 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.694 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.497 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.506 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.398 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.248 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.248 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.625 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.488 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.570 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.482 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.339 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.455 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.406 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.530 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.544 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.622 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.291 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.481 |
MOD_Plk_2-3 | 241 | 247 | PF00069 | 0.706 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.453 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.714 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.640 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.653 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.730 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.434 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.448 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.540 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 320 | 330 | PF00179 | 0.707 |
MOD_SUMO_rev_2 | 487 | 495 | PF00179 | 0.543 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 305 | 308 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.531 |
TRG_ER_diLys_1 | 494 | 498 | PF00400 | 0.557 |
TRG_NLS_MonoExtC_3 | 303 | 308 | PF00514 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF88 | Leptomonas seymouri | 58% | 100% |
A0A0S4J9Z5 | Bodo saltans | 38% | 100% |
A0A1X0NH58 | Trypanosomatidae | 39% | 100% |
A0A3Q8IHU4 | Leishmania donovani | 88% | 100% |
A0A3R7KY85 | Trypanosoma rangeli | 39% | 100% |
A4HG19 | Leishmania braziliensis | 76% | 98% |
A4I340 | Leishmania infantum | 88% | 100% |
C9ZJL2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9ACV9 | Leishmania major | 84% | 98% |
Q28IV3 | Xenopus tropicalis | 25% | 76% |
Q5ZKQ3 | Gallus gallus | 23% | 75% |
Q6NU95 | Xenopus laevis | 25% | 75% |
V5AR46 | Trypanosoma cruzi | 38% | 100% |