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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4I5Y4
Term | Name | Level | Count |
---|---|---|---|
GO:0010960 | magnesium ion homeostasis | 8 | 11 |
GO:0042592 | homeostatic process | 3 | 11 |
GO:0048878 | chemical homeostasis | 4 | 11 |
GO:0050801 | monoatomic ion homeostasis | 5 | 11 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 11 |
GO:0055080 | monoatomic cation homeostasis | 6 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0065008 | regulation of biological quality | 2 | 11 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 11 |
GO:0098771 | inorganic ion homeostasis | 6 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.540 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.130 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.267 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.241 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.441 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.469 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 438 | 444 | PF00134 | 0.362 |
DOC_MAPK_gen_1 | 287 | 295 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 403 | 410 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 287 | 295 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 403 | 410 | PF00069 | 0.460 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.324 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.403 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 323 | 331 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 443 | 449 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 494 | 499 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.441 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.506 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.410 |
LIG_CtBP_PxDLS_1 | 445 | 450 | PF00389 | 0.375 |
LIG_EH1_1 | 288 | 296 | PF00400 | 0.343 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.168 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.124 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.256 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.309 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.457 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.505 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.455 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.526 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.306 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.528 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.415 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.293 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.244 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.443 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.400 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.505 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.291 |
LIG_LIR_Apic_2 | 301 | 307 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 47 | 54 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.214 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.214 |
LIG_MAD2 | 162 | 170 | PF02301 | 0.209 |
LIG_MAD2 | 52 | 60 | PF02301 | 0.466 |
LIG_NBox_RRM_1 | 138 | 148 | PF00076 | 0.309 |
LIG_PCNA_yPIPBox_3 | 384 | 393 | PF02747 | 0.319 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.378 |
LIG_Rb_pABgroove_1 | 96 | 104 | PF01858 | 0.352 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.257 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.257 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.414 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.267 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.324 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.420 |
LIG_SH3_CIN85_PxpxPR_1 | 451 | 456 | PF14604 | 0.389 |
LIG_SUMO_SIM_anti_2 | 362 | 368 | PF11976 | 0.213 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.206 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.208 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 388 | 394 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 93 | 100 | PF11976 | 0.260 |
LIG_SxIP_EBH_1 | 432 | 443 | PF03271 | 0.372 |
LIG_TRAF2_2 | 221 | 226 | PF00917 | 0.401 |
LIG_TYR_ITSM | 272 | 279 | PF00017 | 0.349 |
LIG_UBA3_1 | 69 | 74 | PF00899 | 0.323 |
MOD_CDC14_SPxK_1 | 477 | 480 | PF00782 | 0.501 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.378 |
MOD_CDK_SPxK_1 | 474 | 480 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 449 | 456 | PF00069 | 0.495 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.323 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.364 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.653 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.431 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.214 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.472 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.564 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.408 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.542 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.646 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.676 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.689 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.532 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.439 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.543 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.521 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.695 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.288 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.756 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.342 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.523 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.696 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.533 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.245 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.427 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.412 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.479 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.318 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.718 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.619 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.263 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.757 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.145 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.371 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.557 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.139 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.446 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.372 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.490 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.488 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.479 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.263 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.286 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.286 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.371 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.309 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.451 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.492 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.358 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.563 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.342 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.643 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.505 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.337 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.556 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.292 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.665 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.390 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.314 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.321 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.598 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.350 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.358 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.647 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.633 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.489 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.584 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.323 |
MOD_SUMO_rev_2 | 226 | 232 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 477 | 486 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_3 | 189 | 195 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M9 | Leptomonas seymouri | 26% | 100% |
A0A0N1I470 | Leptomonas seymouri | 66% | 98% |
A0A0N1PDI6 | Leptomonas seymouri | 24% | 83% |
A0A0S4IPA6 | Bodo saltans | 42% | 100% |
A0A0S4JSF9 | Bodo saltans | 25% | 93% |
A0A1X0NRR8 | Trypanosomatidae | 23% | 100% |
A0A1X0P1F1 | Trypanosomatidae | 46% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 27% | 88% |
A0A3Q8IC75 | Leishmania donovani | 100% | 100% |
A0A3Q8IL77 | Leishmania donovani | 24% | 82% |
A0A3Q8ITK0 | Leishmania donovani | 25% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 45% | 100% |
A0A422NS01 | Trypanosoma rangeli | 25% | 88% |
A4HAY2 | Leishmania braziliensis | 25% | 85% |
A4HIN7 | Leishmania braziliensis | 80% | 99% |
A4I8C4 | Leishmania infantum | 25% | 100% |
A4IA41 | Leishmania infantum | 24% | 82% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 89% |
D0A017 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 68% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 82% |
Q12296 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 71% |
Q4Q2T0 | Leishmania major | 24% | 82% |
Q4Q6Y7 | Leishmania major | 97% | 100% |
Q4V3C7 | Arabidopsis thaliana | 32% | 100% |
Q67XQ0 | Arabidopsis thaliana | 33% | 100% |
Q8VZI2 | Arabidopsis thaliana | 28% | 100% |
Q9USJ3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 73% |
Q9ZQR4 | Arabidopsis thaliana | 29% | 100% |
V5BKR5 | Trypanosoma cruzi | 23% | 87% |
V5DM70 | Trypanosoma cruzi | 25% | 100% |
V5DNW3 | Trypanosoma cruzi | 46% | 100% |