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 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H7A7
Term | Name | Level | Count |
---|---|---|---|
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006766 | vitamin metabolic process | 3 | 11 |
GO:0006767 | water-soluble vitamin metabolic process | 4 | 11 |
GO:0006790 | sulfur compound metabolic process | 3 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009110 | vitamin biosynthetic process | 4 | 11 |
GO:0009229 | thiamine diphosphate biosynthetic process | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0042357 | thiamine diphosphate metabolic process | 4 | 11 |
GO:0042364 | water-soluble vitamin biosynthetic process | 5 | 11 |
GO:0042723 | thiamine-containing compound metabolic process | 4 | 11 |
GO:0042724 | thiamine-containing compound biosynthetic process | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044283 | small molecule biosynthetic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0072527 | pyrimidine-containing compound metabolic process | 4 | 11 |
GO:0072528 | pyrimidine-containing compound biosynthetic process | 5 | 11 |
GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004788 | thiamine diphosphokinase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016778 | diphosphotransferase activity | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0019842 | vitamin binding | 3 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0030975 | thiamine binding | 3 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0043178 | alcohol binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:1901681 | sulfur compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.432 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.498 |
CLV_PCSK_FUR_1 | 218 | 222 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.441 |
DEG_SCF_FBW7_1 | 335 | 340 | PF00400 | 0.392 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.453 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.461 |
DEG_SPOP_SBC_1 | 29 | 33 | PF00917 | 0.382 |
DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.317 |
DOC_MAPK_DCC_7 | 234 | 242 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 380 | 390 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 465 | 471 | PF00149 | 0.478 |
DOC_PP2B_LxvP_1 | 268 | 271 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 526 | 529 | PF13499 | 0.425 |
DOC_PP4_FxxP_1 | 407 | 410 | PF00568 | 0.280 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.439 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 365 | 382 | PF00022 | 0.257 |
LIG_APCC_ABBAyCdc20_2 | 198 | 204 | PF00400 | 0.506 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.679 |
LIG_EVH1_2 | 520 | 524 | PF00568 | 0.351 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.517 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.349 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.492 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.565 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.527 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.314 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.542 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.480 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.409 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.487 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.546 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.270 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.618 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.431 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.470 |
LIG_IBAR_NPY_1 | 102 | 104 | PF08397 | 0.335 |
LIG_LIR_Apic_2 | 405 | 410 | PF02991 | 0.266 |
LIG_LIR_Apic_2 | 412 | 416 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 109 | 120 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 65 | 70 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.283 |
LIG_PTB_Apo_2 | 99 | 106 | PF02174 | 0.403 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.458 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.595 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.499 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.334 |
LIG_SH2_GRB2like | 7 | 10 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 66 | 69 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.485 |
LIG_SH3_2 | 433 | 438 | PF14604 | 0.380 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.695 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.402 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.538 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.416 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.584 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.637 |
LIG_SUMO_SIM_anti_2 | 238 | 244 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 481 | 488 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 49 | 55 | PF11976 | 0.383 |
LIG_TRFH_1 | 407 | 411 | PF08558 | 0.296 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.373 |
LIG_UBA3_1 | 387 | 392 | PF00899 | 0.364 |
LIG_WW_3 | 414 | 418 | PF00397 | 0.412 |
MOD_CDC14_SPxK_1 | 414 | 417 | PF00782 | 0.408 |
MOD_CDK_SPxK_1 | 139 | 145 | PF00069 | 0.379 |
MOD_CDK_SPxK_1 | 411 | 417 | PF00069 | 0.382 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.530 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.542 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.358 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.365 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.546 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.642 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.458 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.468 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.492 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.694 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.291 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.734 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.513 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.726 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.686 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.515 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.521 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.486 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.539 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.649 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.560 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.669 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.525 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.533 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.602 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.629 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.343 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.616 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.436 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.406 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.449 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.608 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.622 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.604 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.365 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.610 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.360 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.349 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.302 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.330 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.574 |
MOD_PKB_1 | 274 | 282 | PF00069 | 0.458 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.626 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.464 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.486 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.466 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.416 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.393 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.239 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.379 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.568 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.545 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.403 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.330 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.346 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.738 |
TRG_DiLeu_BaEn_1 | 441 | 446 | PF01217 | 0.259 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.345 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFZ8 | Leptomonas seymouri | 44% | 100% |
A0A1X0NMY7 | Trypanosomatidae | 30% | 100% |
A0A3Q8IBS6 | Leishmania donovani | 70% | 99% |
A0A422N0R9 | Trypanosoma rangeli | 29% | 100% |
A4HVQ2 | Leishmania infantum | 71% | 100% |
D0A6I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9APE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QG30 | Leishmania major | 68% | 100% |
V5ARR9 | Trypanosoma cruzi | 28% | 100% |