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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005615 | extracellular space | 2 | 1 |
Related structures:
AlphaFold database: E9B0G8
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
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: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 |
GO:0003756 | protein disulfide isomerase activity | 3 | 1 |
GO:0016853 | isomerase activity | 2 | 1 |
GO:0016860 | intramolecular oxidoreductase activity | 3 | 1 |
GO:0016864 | intramolecular oxidoreductase activity, transposing S-S bonds | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.423 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 549 | 551 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 549 | 551 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.573 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.283 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.348 |
DOC_MAPK_FxFP_2 | 126 | 129 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 549 | 557 | PF00069 | 0.734 |
DOC_MAPK_MEF2A_6 | 514 | 523 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 549 | 557 | PF00069 | 0.709 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.348 |
DOC_PP2B_PxIxI_1 | 60 | 66 | PF00149 | 0.399 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.256 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.172 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 514 | 520 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.314 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.336 |
LIG_EH_1 | 514 | 518 | PF12763 | 0.325 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.445 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.339 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.279 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.272 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.268 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.375 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.580 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.559 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.345 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.445 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.237 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.391 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.298 |
LIG_LIR_Apic_2 | 123 | 129 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 305 | 312 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 382 | 391 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 402 | 409 | PF02991 | 0.150 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 520 | 525 | PF02991 | 0.269 |
LIG_MLH1_MIPbox_1 | 122 | 126 | PF16413 | 0.297 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.297 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.329 |
LIG_PTB_Apo_2 | 142 | 149 | PF02174 | 0.230 |
LIG_PTB_Apo_2 | 241 | 248 | PF02174 | 0.347 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.290 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.240 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 390 | 394 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.297 |
LIG_SH3_1 | 550 | 556 | PF00018 | 0.724 |
LIG_SH3_2 | 438 | 443 | PF14604 | 0.329 |
LIG_SH3_2 | 553 | 558 | PF14604 | 0.723 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.297 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.322 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.724 |
LIG_SUMO_SIM_anti_2 | 524 | 530 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 41 | 49 | PF11976 | 0.355 |
LIG_TRFH_1 | 125 | 129 | PF08558 | 0.348 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.290 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.336 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.304 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.172 |
MOD_CDK_SPK_2 | 326 | 331 | PF00069 | 0.353 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.453 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.361 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.375 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.220 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.297 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.369 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.546 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.565 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.565 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.489 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.518 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.550 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.388 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.442 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.568 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.303 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.499 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.352 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.640 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.530 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.414 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.326 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.354 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.429 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.461 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.340 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.274 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.387 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.345 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.433 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.324 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.346 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.497 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.407 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.320 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.272 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.346 |
MOD_Plk_2-3 | 107 | 113 | PF00069 | 0.218 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.348 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.309 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.172 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.333 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.353 |
MOD_SUMO_rev_2 | 150 | 159 | PF00179 | 0.448 |
TRG_AP2beta_CARGO_1 | 382 | 392 | PF09066 | 0.342 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.235 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 557 | 560 | PF00400 | 0.721 |
TRG_NLS_MonoCore_2 | 548 | 553 | PF00514 | 0.712 |
TRG_NLS_MonoExtC_3 | 548 | 553 | PF00514 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 33 | 38 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H4 | Leptomonas seymouri | 47% | 97% |
A0A0S4ILW1 | Bodo saltans | 31% | 72% |
A0A1X0P2E7 | Trypanosomatidae | 34% | 100% |
A0A3S7X306 | Leishmania donovani | 86% | 100% |
A0A422NMK4 | Trypanosoma rangeli | 36% | 100% |
A4HHZ4 | Leishmania braziliensis | 66% | 99% |
A4I571 | Leishmania infantum | 86% | 100% |
C9ZQJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4Q7R5 | Leishmania major | 84% | 98% |