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: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 10, no: 1 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005788 | endoplasmic reticulum lumen | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005783 | endoplasmic reticulum | 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: A4HAT2
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003756 | protein disulfide isomerase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016860 | intramolecular oxidoreductase activity | 3 | 12 |
GO:0016864 | intramolecular oxidoreductase activity, transposing S-S bonds | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0015035 | protein-disulfide reductase activity | 3 | 1 |
GO:0015036 | disulfide oxidoreductase activity | 4 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.530 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.472 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.365 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.548 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.406 |
DOC_CYCLIN_RxL_1 | 189 | 199 | PF00134 | 0.276 |
DOC_MAPK_DCC_7 | 175 | 184 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 190 | 198 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 317 | 327 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 341 | 351 | PF00069 | 0.519 |
DOC_MAPK_HePTP_8 | 172 | 184 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 190 | 198 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 344 | 351 | PF00069 | 0.488 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.338 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.706 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.204 |
LIG_Actin_WH2_2 | 210 | 226 | PF00022 | 0.435 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.443 |
LIG_Clathr_ClatBox_1 | 348 | 352 | PF01394 | 0.380 |
LIG_Clathr_ClatBox_1 | 425 | 429 | PF01394 | 0.290 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.545 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.469 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.485 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.442 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.526 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.433 |
LIG_HP1_1 | 53 | 57 | PF01393 | 0.425 |
LIG_LIR_Apic_2 | 309 | 314 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 234 | 240 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 72 | 80 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.323 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.552 |
LIG_PCNA_yPIPBox_3 | 216 | 224 | PF02747 | 0.377 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.338 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.338 |
LIG_SH2_NCK_1 | 225 | 229 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.381 |
LIG_SH2_STAT3 | 125 | 128 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.476 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.487 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.492 |
LIG_SUMO_SIM_anti_2 | 383 | 390 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 180 | 186 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 371 | 377 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 424 | 429 | PF11976 | 0.460 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.332 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.373 |
LIG_UBA3_1 | 167 | 175 | PF00899 | 0.417 |
LIG_UBA3_1 | 181 | 190 | PF00899 | 0.498 |
LIG_UBA3_1 | 360 | 367 | PF00899 | 0.408 |
MOD_CDC14_SPxK_1 | 163 | 166 | PF00782 | 0.302 |
MOD_CDK_SPK_2 | 160 | 165 | PF00069 | 0.298 |
MOD_CDK_SPK_2 | 185 | 190 | PF00069 | 0.427 |
MOD_CDK_SPK_2 | 301 | 306 | PF00069 | 0.511 |
MOD_CDK_SPxK_1 | 160 | 166 | PF00069 | 0.299 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.427 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.425 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.452 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.377 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.460 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.675 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.448 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.688 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.401 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.454 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.419 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.500 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.599 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.557 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.297 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.477 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.375 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.358 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.618 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.389 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.550 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.417 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.434 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.646 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.539 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.560 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.321 |
MOD_N-GLC_2 | 261 | 263 | PF02516 | 0.317 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.628 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.408 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.348 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.477 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.449 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.500 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.442 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.309 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.282 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.446 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.429 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.425 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.646 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.424 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.204 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.527 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.377 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.374 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.655 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.561 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.299 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.395 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.483 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.454 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.448 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.545 |
MOD_SUMO_rev_2 | 154 | 159 | PF00179 | 0.319 |
MOD_SUMO_rev_2 | 273 | 283 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 7 | 12 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.412 |
TRG_NES_CRM1_1 | 358 | 371 | PF08389 | 0.442 |
TRG_NLS_MonoExtN_4 | 314 | 321 | PF00514 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 417 | 422 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y0 | Leptomonas seymouri | 53% | 95% |
A0A0S4J6N7 | Bodo saltans | 36% | 99% |
A0A1X0PAY2 | Trypanosomatidae | 39% | 100% |
A0A3Q8IL31 | Leishmania donovani | 75% | 100% |
A4I9Z2 | Leishmania infantum | 75% | 100% |
C9ZMN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AY45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B506 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q2Y0 | Leishmania major | 74% | 100% |
V5BFX1 | Trypanosoma cruzi | 38% | 98% |