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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HH24
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.451 |
CLV_PCSK_FUR_1 | 227 | 231 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.320 |
CLV_Separin_Metazoa | 202 | 206 | PF03568 | 0.310 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.584 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.561 |
DEG_MDM2_SWIB_1 | 118 | 125 | PF02201 | 0.444 |
DEG_SCF_FBW7_1 | 488 | 493 | PF00400 | 0.380 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.391 |
DEG_SPOP_SBC_1 | 501 | 505 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 511 | 515 | PF00917 | 0.390 |
DOC_CDC14_PxL_1 | 303 | 311 | PF14671 | 0.457 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.354 |
DOC_CYCLIN_RxL_1 | 399 | 407 | PF00134 | 0.478 |
DOC_CYCLIN_RxL_1 | 4 | 14 | PF00134 | 0.591 |
DOC_CYCLIN_yCln2_LP_2 | 125 | 131 | PF00134 | 0.380 |
DOC_MAPK_gen_1 | 165 | 174 | PF00069 | 0.610 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 558 | 568 | PF00069 | 0.654 |
DOC_MAPK_gen_1 | 59 | 67 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 6 | 12 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 314 | 322 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.546 |
DOC_MAPK_NFAT4_5 | 341 | 349 | PF00069 | 0.591 |
DOC_PP1_RVXF_1 | 546 | 553 | PF00149 | 0.650 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.372 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 268 | 272 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 453 | 460 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 484 | 489 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 499 | 508 | PF00244 | 0.444 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.233 |
LIG_APCC_ABBA_1 | 27 | 32 | PF00400 | 0.233 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.713 |
LIG_CaM_IQ_9 | 550 | 566 | PF13499 | 0.666 |
LIG_Clathr_ClatBox_1 | 39 | 43 | PF01394 | 0.495 |
LIG_eIF4E_1 | 34 | 40 | PF01652 | 0.459 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.374 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.394 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.590 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.505 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.309 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.353 |
LIG_LIR_Apic_2 | 326 | 330 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 111 | 120 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 140 | 148 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 262 | 267 | PF02991 | 0.544 |
LIG_LIR_LC3C_4 | 319 | 322 | PF02991 | 0.233 |
LIG_LIR_LC3C_4 | 534 | 538 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.429 |
LIG_NRBOX | 345 | 351 | PF00104 | 0.394 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.414 |
LIG_Pex14_1 | 539 | 543 | PF04695 | 0.534 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.375 |
LIG_Pex14_2 | 26 | 30 | PF04695 | 0.444 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.471 |
LIG_SH2_GRB2like | 542 | 545 | PF00017 | 0.636 |
LIG_SH2_NCK_1 | 288 | 292 | PF00017 | 0.272 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.485 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.382 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.444 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.443 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.325 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.630 |
LIG_SUMO_SIM_anti_2 | 356 | 362 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 455 | 461 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 467 | 474 | PF11976 | 0.650 |
LIG_SUMO_SIM_anti_2 | 519 | 525 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 519 | 525 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.588 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.697 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.686 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.463 |
MOD_CDC14_SPxK_1 | 198 | 201 | PF00782 | 0.456 |
MOD_CDK_SPK_2 | 195 | 200 | PF00069 | 0.429 |
MOD_CDK_SPK_2 | 486 | 491 | PF00069 | 0.393 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.435 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.408 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.392 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.725 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.233 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.524 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.534 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.485 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.348 |
MOD_Cter_Amidation | 339 | 342 | PF01082 | 0.332 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.561 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.436 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.398 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.403 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.505 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.528 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.599 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.674 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.310 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.399 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.666 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.662 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.457 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.426 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.473 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.564 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.494 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.404 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.235 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.621 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.481 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.414 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.464 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.401 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.358 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.558 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.354 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.485 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.233 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.485 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.432 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.615 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.665 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.544 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.411 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.465 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.733 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.690 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.368 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.622 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.405 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.338 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.446 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.394 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.312 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.250 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.435 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.350 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.501 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.372 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.698 |
MOD_SUMO_for_1 | 199 | 202 | PF00179 | 0.345 |
TRG_DiLeu_BaEn_2 | 261 | 267 | PF01217 | 0.617 |
TRG_DiLeu_BaLyEn_6 | 399 | 404 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 558 | 560 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVM9 | Leptomonas seymouri | 42% | 100% |
A0A1X0NZT8 | Trypanosomatidae | 23% | 100% |
A0A3Q8IH23 | Leishmania donovani | 73% | 100% |
A0A3R7KT94 | Trypanosoma rangeli | 26% | 100% |
A4I453 | Leishmania infantum | 73% | 100% |
C9ZKQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9ADL8 | Leishmania major | 72% | 100% |
E9AM63 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |