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: A0A3Q8IHU4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 299 | 303 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.594 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.312 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.291 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DEG_SPOP_SBC_1 | 219 | 223 | PF00917 | 0.469 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.772 |
DEG_SPOP_SBC_1 | 350 | 354 | PF00917 | 0.781 |
DOC_CKS1_1 | 370 | 375 | PF01111 | 0.536 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.539 |
DOC_MAPK_gen_1 | 228 | 234 | PF00069 | 0.633 |
DOC_MAPK_gen_1 | 298 | 308 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.479 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.380 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.601 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.526 |
LIG_APCC_ABBA_1 | 449 | 454 | PF00400 | 0.436 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.472 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.457 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.472 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.426 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.720 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.526 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.533 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.664 |
LIG_LIR_Gen_1 | 375 | 383 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 394 | 402 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.434 |
LIG_PCNA_PIPBox_1 | 389 | 398 | PF02747 | 0.557 |
LIG_Pex14_2 | 379 | 383 | PF04695 | 0.463 |
LIG_SH2_GRB2like | 131 | 134 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.371 |
LIG_SH2_PTP2 | 396 | 399 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.463 |
LIG_SH3_1 | 469 | 475 | PF00018 | 0.597 |
LIG_SH3_2 | 472 | 477 | PF14604 | 0.617 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.753 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.549 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.651 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 304 | 313 | PF11976 | 0.663 |
LIG_SUMO_SIM_anti_2 | 463 | 470 | PF11976 | 0.459 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.538 |
LIG_TRAF2_1 | 257 | 260 | PF00917 | 0.662 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.626 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.781 |
LIG_UBA3_1 | 417 | 426 | PF00899 | 0.452 |
LIG_WRC_WIRS_1 | 425 | 430 | PF05994 | 0.538 |
LIG_WW_2 | 337 | 340 | PF00397 | 0.549 |
MOD_CDK_SPK_2 | 369 | 374 | PF00069 | 0.493 |
MOD_CDK_SPxK_1 | 471 | 477 | PF00069 | 0.529 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.482 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.672 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.693 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.679 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.485 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.507 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.637 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.466 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.530 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.755 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.306 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.501 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.551 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.551 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.572 |
MOD_GlcNHglycan | 195 | 199 | PF01048 | 0.435 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.726 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.688 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.725 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.721 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.531 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.612 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.636 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.603 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.679 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.694 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.663 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.519 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.516 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.411 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.263 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.263 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.642 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.505 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.544 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.565 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.500 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.321 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.466 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.581 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.536 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.536 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.606 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.561 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.637 |
MOD_Plk_2-3 | 236 | 242 | PF00069 | 0.727 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.733 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.674 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.629 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.672 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.457 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.463 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.529 |
MOD_SUMO_rev_2 | 13 | 23 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 312 | 322 | PF00179 | 0.727 |
MOD_SUMO_rev_2 | 478 | 486 | PF00179 | 0.549 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.538 |
TRG_ER_diLys_1 | 485 | 489 | PF00400 | 0.561 |
TRG_NLS_Bipartite_1 | 212 | 233 | PF00514 | 0.649 |
TRG_NLS_MonoCore_2 | 227 | 232 | PF00514 | 0.627 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.578 |
TRG_NLS_MonoExtN_4 | 228 | 233 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.274 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF88 | Leptomonas seymouri | 62% | 99% |
A0A0S4J9Z5 | Bodo saltans | 40% | 100% |
A0A1X0NH58 | Trypanosomatidae | 39% | 100% |
A0A3R7KY85 | Trypanosoma rangeli | 39% | 100% |
A4HG19 | Leishmania braziliensis | 82% | 99% |
A4I340 | Leishmania infantum | 99% | 100% |
C9ZJL2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACV9 | Leishmania major | 93% | 100% |
E9AZE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q28IV3 | Xenopus tropicalis | 25% | 74% |
Q5ZKQ3 | Gallus gallus | 24% | 74% |
Q68FQ7 | Rattus norvegicus | 26% | 74% |
Q6NU95 | Xenopus laevis | 26% | 74% |
Q9D706 | Mus musculus | 25% | 74% |
V5AR46 | Trypanosoma cruzi | 38% | 100% |