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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QHH6
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 11 |
GO:0006066 | alcohol metabolic process | 3 | 11 |
GO:0006071 | glycerol metabolic process | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016052 | carbohydrate catabolic process | 4 | 2 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019400 | alditol metabolic process | 4 | 11 |
GO:0019405 | alditol catabolic process | 5 | 2 |
GO:0019563 | glycerol catabolic process | 6 | 2 |
GO:0019751 | polyol metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 11 |
GO:0044275 | obsolete cellular carbohydrate catabolic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044282 | small molecule catabolic process | 3 | 2 |
GO:0046164 | alcohol catabolic process | 4 | 2 |
GO:0046174 | polyol catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 11 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004371 | glycerone kinase activity | 5 | 11 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.520 |
CLV_MEL_PAP_1 | 183 | 189 | PF00089 | 0.391 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.255 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.205 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.239 |
DOC_ANK_TNKS_1 | 98 | 105 | PF00023 | 0.205 |
DOC_CDC14_PxL_1 | 429 | 437 | PF14671 | 0.444 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.370 |
DOC_PP1_RVXF_1 | 328 | 335 | PF00149 | 0.420 |
DOC_PP2B_PxIxI_1 | 104 | 110 | PF00149 | 0.318 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.315 |
DOC_PP4_FxxP_1 | 348 | 351 | PF00568 | 0.404 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.273 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.159 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.318 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.305 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.520 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.273 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 442 | 448 | PF00244 | 0.569 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.273 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.388 |
LIG_Clathr_ClatBox_1 | 398 | 402 | PF01394 | 0.442 |
LIG_DLG_GKlike_1 | 173 | 180 | PF00625 | 0.399 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.330 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.378 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.449 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.267 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.399 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.425 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.273 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.486 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.273 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.528 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.429 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.338 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.292 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.273 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.430 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.430 |
LIG_Integrin_RGD_1 | 507 | 509 | PF01839 | 0.258 |
LIG_LIR_Apic_2 | 79 | 84 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.462 |
LIG_LIR_LC3C_4 | 575 | 578 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.449 |
LIG_Pex14_2 | 230 | 234 | PF04695 | 0.305 |
LIG_PTB_Apo_2 | 117 | 124 | PF02174 | 0.292 |
LIG_PTB_Phospho_1 | 117 | 123 | PF10480 | 0.388 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.292 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.520 |
LIG_SH2_GRB2like | 404 | 407 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.273 |
LIG_SH3_1 | 99 | 105 | PF00018 | 0.221 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.400 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.502 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.444 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.318 |
LIG_SUMO_SIM_anti_2 | 320 | 325 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 424 | 430 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 511 | 517 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 320 | 329 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 511 | 517 | PF11976 | 0.430 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.413 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.292 |
LIG_UBA3_1 | 107 | 112 | PF00899 | 0.351 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.273 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.445 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.567 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.318 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.292 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.462 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.334 |
MOD_Cter_Amidation | 567 | 570 | PF01082 | 0.320 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.592 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.386 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.252 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.399 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.599 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.244 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.244 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.230 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.321 |
MOD_GlcNHglycan | 501 | 505 | PF01048 | 0.261 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.320 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.271 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.179 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.292 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.205 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.280 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.212 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.316 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.584 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.299 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.399 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.292 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.437 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.476 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.454 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.492 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.355 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.292 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.565 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.442 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.430 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.488 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.466 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.400 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.367 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.312 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.388 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.399 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.399 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.515 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.452 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.273 |
MOD_SUMO_rev_2 | 559 | 567 | PF00179 | 0.512 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.444 |
TRG_NES_CRM1_1 | 315 | 329 | PF08389 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0Z1 | Leptomonas seymouri | 75% | 100% |
A0A0S4IPA3 | Bodo saltans | 43% | 96% |
A0A1X0P659 | Trypanosomatidae | 55% | 100% |
A0A3S5H6F7 | Leishmania donovani | 95% | 100% |
A0A422NR38 | Trypanosoma rangeli | 56% | 100% |
A0QXE4 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 31% | 100% |
A0R758 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 32% | 100% |
A4H621 | Leishmania braziliensis | 83% | 90% |
A4HUE9 | Leishmania infantum | 95% | 100% |
E9AN48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
F1RKQ4 | Sus scrofa | 35% | 100% |
O04059 | Solanum lycopersicum | 34% | 99% |
O13902 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O60017 | Pichia angusta | 32% | 97% |
O74192 | Komagataella pastoris | 31% | 97% |
O74215 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P43550 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P45510 | Citrobacter freundii | 33% | 100% |
P54838 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q3LXA3 | Homo sapiens | 33% | 100% |
Q4KLZ6 | Rattus norvegicus | 33% | 100% |
Q55EE0 | Dictyostelium discoideum | 28% | 91% |
Q58DK4 | Bos taurus | 33% | 100% |
Q6D8V6 | Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) | 31% | 100% |
Q8VC30 | Mus musculus | 34% | 100% |
V5C2U9 | Trypanosoma cruzi | 53% | 100% |