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: A4HVQ2
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: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 |
GO:0016310 | phosphorylation | 5 | 9 |
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: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 |
GO:0016301 | kinase activity | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.430 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.388 |
CLV_PCSK_FUR_1 | 218 | 222 | PF00082 | 0.520 |
CLV_PCSK_FUR_1 | 327 | 331 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.464 |
CLV_PCSK_PC7_1 | 118 | 124 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.334 |
CLV_Separin_Metazoa | 182 | 186 | PF03568 | 0.568 |
DEG_APCC_DBOX_1 | 328 | 336 | PF00400 | 0.395 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.531 |
DOC_CYCLIN_RxL_1 | 326 | 336 | PF00134 | 0.397 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.522 |
DOC_PP1_RVXF_1 | 196 | 203 | PF00149 | 0.462 |
DOC_PP1_RVXF_1 | 465 | 471 | PF00149 | 0.491 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.435 |
DOC_PP2B_LxvP_1 | 526 | 529 | PF13499 | 0.438 |
DOC_PP2B_PxIxI_1 | 355 | 361 | PF00149 | 0.345 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.672 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.462 |
LIG_APCC_ABBAyCdc20_2 | 198 | 204 | PF00400 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.683 |
LIG_BIR_III_2 | 180 | 184 | PF00653 | 0.558 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.392 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.401 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_2 | 249 | 255 | PF00533 | 0.412 |
LIG_EVH1_2 | 520 | 524 | PF00568 | 0.359 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.402 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.602 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.489 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.536 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.413 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.347 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.509 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.484 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.422 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.419 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.557 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.474 |
LIG_GBD_Chelix_1 | 142 | 150 | PF00786 | 0.329 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 238 | 246 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 65 | 70 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.356 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.454 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.493 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.425 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.385 |
LIG_SH2_PTP2 | 66 | 69 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.372 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.539 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.479 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.399 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.409 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.585 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.593 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.673 |
LIG_SUMO_SIM_par_1 | 208 | 215 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 481 | 488 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 49 | 55 | PF11976 | 0.380 |
LIG_TRFH_1 | 240 | 244 | PF08558 | 0.362 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.397 |
LIG_UBA3_1 | 387 | 392 | PF00899 | 0.384 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.568 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.467 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.325 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.495 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.550 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.571 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.436 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.695 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.392 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.684 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.451 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.633 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.539 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.538 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.331 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.681 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.580 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.466 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.408 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.696 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.473 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.710 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.534 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.598 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.346 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.416 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.554 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.524 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.398 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.579 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.382 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.308 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.348 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.609 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.598 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.691 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.528 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.419 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.441 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.542 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.435 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.401 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.351 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.554 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.565 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.484 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.354 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.705 |
TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.498 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 199 | 204 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFZ8 | Leptomonas seymouri | 43% | 100% |
A0A1X0NMY7 | Trypanosomatidae | 30% | 100% |
A0A3Q8IBS6 | Leishmania donovani | 99% | 99% |
A0A422N0R9 | Trypanosoma rangeli | 27% | 100% |
A4H7A7 | Leishmania braziliensis | 71% | 100% |
D0A6I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9APE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QG30 | Leishmania major | 88% | 100% |
V5ARR9 | Trypanosoma cruzi | 26% | 100% |