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: A4HHZ4
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 | 114 | 116 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 542 | 544 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.210 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.287 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.375 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.320 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.224 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.200 |
DOC_MAPK_gen_1 | 403 | 411 | PF00069 | 0.252 |
DOC_MAPK_gen_1 | 542 | 550 | PF00069 | 0.714 |
DOC_MAPK_MEF2A_6 | 403 | 411 | PF00069 | 0.188 |
DOC_MAPK_MEF2A_6 | 542 | 550 | PF00069 | 0.688 |
DOC_PP1_RVXF_1 | 329 | 336 | PF00149 | 0.324 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.243 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.169 |
DOC_PP2B_PxIxI_1 | 60 | 66 | PF00149 | 0.369 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.208 |
DOC_SPAK_OSR1_1 | 459 | 463 | PF12202 | 0.227 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.640 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.327 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 334 | 343 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 459 | 469 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 6 | 16 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.288 |
LIG_Actin_WH2_2 | 520 | 536 | PF00022 | 0.297 |
LIG_AP2alpha_1 | 36 | 40 | PF02296 | 0.332 |
LIG_APCC_ABBAyCdc20_2 | 434 | 440 | PF00400 | 0.212 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.458 |
LIG_Clathr_ClatBox_1 | 256 | 260 | PF01394 | 0.239 |
LIG_CtBP_PxDLS_1 | 129 | 133 | PF00389 | 0.317 |
LIG_eIF4E_1 | 251 | 257 | PF01652 | 0.265 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.369 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.241 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.310 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.489 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.335 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.190 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.422 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.379 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.347 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.271 |
LIG_LIR_Gen_1 | 123 | 132 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 13 | 23 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 305 | 313 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 394 | 401 | PF02991 | 0.126 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.215 |
LIG_MYND_1 | 441 | 445 | PF01753 | 0.230 |
LIG_Pex14_2 | 36 | 40 | PF04695 | 0.370 |
LIG_PTB_Apo_2 | 296 | 303 | PF02174 | 0.314 |
LIG_PTB_Phospho_1 | 296 | 302 | PF10480 | 0.319 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.263 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 382 | 386 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.601 |
LIG_SH3_1 | 543 | 549 | PF00018 | 0.703 |
LIG_SH3_2 | 546 | 551 | PF14604 | 0.693 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.703 |
LIG_SUMO_SIM_anti_2 | 253 | 258 | PF11976 | 0.206 |
LIG_SUMO_SIM_anti_2 | 523 | 528 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 41 | 48 | PF11976 | 0.324 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.169 |
LIG_TRFH_1 | 125 | 129 | PF08558 | 0.322 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.263 |
LIG_TYR_ITSM | 247 | 254 | PF00017 | 0.257 |
LIG_UBA3_1 | 126 | 135 | PF00899 | 0.235 |
MOD_CDK_SPK_2 | 326 | 331 | PF00069 | 0.327 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.256 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.371 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.350 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.395 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.439 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.511 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.606 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.534 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.476 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.498 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.463 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.491 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.362 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.356 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.343 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.414 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.278 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.464 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.322 |
MOD_LATS_1 | 332 | 338 | PF00433 | 0.217 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.586 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.585 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.265 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.292 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.402 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.424 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.310 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.348 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.327 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.396 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.302 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.475 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.324 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.513 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.298 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.474 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.379 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.433 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.230 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.320 |
MOD_Plk_2-3 | 107 | 113 | PF00069 | 0.191 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.465 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.323 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.338 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.380 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.268 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.225 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.305 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.328 |
TRG_AP2beta_CARGO_1 | 374 | 384 | PF09066 | 0.310 |
TRG_DiLeu_BaEn_4 | 111 | 117 | PF01217 | 0.169 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.213 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.169 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.617 |
TRG_NLS_Bipartite_1 | 420 | 438 | PF00514 | 0.247 |
TRG_NLS_MonoCore_2 | 541 | 546 | PF00514 | 0.687 |
TRG_NLS_MonoExtC_3 | 541 | 546 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 431 | 438 | PF00514 | 0.235 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 331 | 336 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H4 | Leptomonas seymouri | 48% | 96% |
A0A0S4ILW1 | Bodo saltans | 29% | 72% |
A0A1X0P2E7 | Trypanosomatidae | 36% | 100% |
A0A3S7X306 | Leishmania donovani | 67% | 99% |
A0A422NMK4 | Trypanosoma rangeli | 39% | 100% |
A4I571 | Leishmania infantum | 67% | 99% |
C9ZQJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B0G8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 99% |
Q4Q7R5 | Leishmania major | 68% | 100% |
Q6IUU3 | Rattus norvegicus | 24% | 74% |