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 | yes | yes: 9, no: 1 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005615 | extracellular space | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0016020 | membrane | 2 | 9 |
Related structures:
AlphaFold database: Q4Q7R5
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003756 | protein disulfide isomerase activity | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0015035 | protein-disulfide reductase activity | 3 | 11 |
GO:0015036 | disulfide oxidoreductase activity | 4 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 11 |
GO:0016670 | oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 2 |
GO:0016860 | intramolecular oxidoreductase activity | 3 | 2 |
GO:0016864 | intramolecular oxidoreductase activity, transposing S-S bonds | 4 | 2 |
GO:0016971 | flavin-linked sulfhydryl oxidase activity | 4 | 11 |
GO:0016972 | thiol oxidase activity | 5 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.443 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.572 |
DOC_CYCLIN_RxL_1 | 143 | 150 | PF00134 | 0.384 |
DOC_CYCLIN_RxL_1 | 193 | 204 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.449 |
DOC_MAPK_FxFP_2 | 126 | 129 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 540 | 548 | PF00069 | 0.744 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 540 | 548 | PF00069 | 0.724 |
DOC_MAPK_NFAT4_5 | 195 | 203 | PF00069 | 0.263 |
DOC_PP1_RVXF_1 | 328 | 335 | PF00149 | 0.372 |
DOC_PP2B_PxIxI_1 | 60 | 66 | PF00149 | 0.395 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.280 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.506 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.278 |
LIG_14-3-3_CanoR_1 | 117 | 122 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 330 | 335 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.334 |
LIG_AP2alpha_1 | 36 | 40 | PF02296 | 0.403 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.630 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.353 |
LIG_Clathr_ClatBox_1 | 507 | 511 | PF01394 | 0.422 |
LIG_EH1_1 | 512 | 520 | PF00400 | 0.386 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.377 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.347 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.396 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.372 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.580 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.311 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.396 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.449 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.439 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.302 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.320 |
LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 312 | 321 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 511 | 521 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.288 |
LIG_MLH1_MIPbox_1 | 122 | 126 | PF16413 | 0.330 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.330 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.335 |
LIG_Pex14_2 | 36 | 40 | PF04695 | 0.410 |
LIG_PTB_Apo_2 | 241 | 248 | PF02174 | 0.364 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.313 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.330 |
LIG_SH3_1 | 541 | 547 | PF00018 | 0.736 |
LIG_SH3_2 | 429 | 434 | PF14604 | 0.354 |
LIG_SH3_2 | 544 | 549 | PF14604 | 0.763 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.383 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.345 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.736 |
LIG_SUMO_SIM_anti_2 | 511 | 518 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 117 | 123 | PF11976 | 0.219 |
LIG_SUMO_SIM_par_1 | 41 | 47 | PF11976 | 0.373 |
LIG_TRFH_1 | 125 | 129 | PF08558 | 0.362 |
LIG_TYR_ITIM | 353 | 358 | PF00017 | 0.313 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.353 |
LIG_WRC_WIRS_1 | 510 | 515 | PF05994 | 0.384 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.351 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.412 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.381 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.430 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.436 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.399 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.420 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.395 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.473 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.455 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.377 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.638 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.587 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.499 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.541 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.561 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.397 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.588 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.366 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.327 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.516 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.393 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.362 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.633 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.591 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.502 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.411 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.326 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.418 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.471 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.345 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.297 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.369 |
MOD_PK_1 | 117 | 123 | PF00069 | 0.219 |
MOD_PK_1 | 490 | 496 | PF00069 | 0.587 |
MOD_PKA_1 | 490 | 496 | PF00069 | 0.427 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.328 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.343 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.360 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.481 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.401 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.463 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.360 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.362 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.319 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.455 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.393 |
MOD_SUMO_rev_2 | 150 | 159 | PF00179 | 0.508 |
TRG_AP2beta_CARGO_1 | 373 | 383 | PF09066 | 0.386 |
TRG_DiLeu_BaEn_2 | 453 | 459 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.734 |
TRG_NLS_MonoCore_2 | 539 | 544 | PF00514 | 0.753 |
TRG_NLS_MonoExtC_3 | 539 | 544 | PF00514 | 0.730 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 33 | 38 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 492 | 496 | PF00026 | 0.736 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H4 | Leptomonas seymouri | 45% | 95% |
A0A0S4ILW1 | Bodo saltans | 29% | 71% |
A0A1X0P2E7 | Trypanosomatidae | 40% | 100% |
A0A3S7X306 | Leishmania donovani | 90% | 99% |
A0A422NMK4 | Trypanosoma rangeli | 37% | 100% |
A4HHZ4 | Leishmania braziliensis | 68% | 100% |
A4I571 | Leishmania infantum | 90% | 99% |
C9ZQJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B0G8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |