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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HNM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006003 | fructose 2,6-bisphosphate metabolic process | 4 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:0016310 | phosphorylation | 5 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003873 | 6-phosphofructo-2-kinase activity | 6 | 6 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008443 | phosphofructokinase activity | 5 | 6 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019200 | carbohydrate kinase activity | 5 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004331 | fructose-2,6-bisphosphate 2-phosphatase activity | 8 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016791 | phosphatase activity | 5 | 4 |
GO:0019203 | carbohydrate phosphatase activity | 6 | 4 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 4 |
GO:0050308 | sugar-phosphatase activity | 7 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.268 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.318 |
CLV_Separin_Metazoa | 38 | 42 | PF03568 | 0.655 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.747 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.556 |
DOC_MAPK_FxFP_2 | 387 | 390 | PF00069 | 0.274 |
DOC_MAPK_gen_1 | 413 | 419 | PF00069 | 0.257 |
DOC_MAPK_MEF2A_6 | 255 | 262 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.247 |
DOC_PP1_RVXF_1 | 145 | 151 | PF00149 | 0.530 |
DOC_PP1_RVXF_1 | 182 | 189 | PF00149 | 0.345 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.289 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.274 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 133 | 142 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 168 | 172 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 264 | 272 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 311 | 315 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 380 | 387 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 471 | 478 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 80 | 88 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 198 | 215 | PF00022 | 0.483 |
LIG_BRCT_BRCA1_1 | 108 | 112 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.448 |
LIG_CtBP_PxDLS_1 | 43 | 47 | PF00389 | 0.617 |
LIG_eIF4E_1 | 373 | 379 | PF01652 | 0.193 |
LIG_EVH1_2 | 258 | 262 | PF00568 | 0.368 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.406 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.373 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.434 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.391 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.334 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.417 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.257 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.399 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.304 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.483 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.683 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.295 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.645 |
LIG_LIR_Apic_2 | 32 | 36 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.451 |
LIG_LYPXL_S_1 | 372 | 376 | PF13949 | 0.308 |
LIG_LYPXL_yS_3 | 373 | 376 | PF13949 | 0.289 |
LIG_PCNA_yPIPBox_3 | 422 | 435 | PF02747 | 0.417 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.356 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.372 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.417 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.439 |
LIG_REV1ctd_RIR_1 | 259 | 268 | PF16727 | 0.274 |
LIG_REV1ctd_RIR_1 | 429 | 435 | PF16727 | 0.417 |
LIG_REV1ctd_RIR_1 | 85 | 95 | PF16727 | 0.315 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.350 |
LIG_SH2_STAT3 | 120 | 123 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.333 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.350 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.534 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.311 |
LIG_SUMO_SIM_anti_2 | 153 | 161 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 393 | 400 | PF11976 | 0.417 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.298 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.308 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.432 |
LIG_TRAF2_2 | 470 | 475 | PF00917 | 0.573 |
LIG_TYR_ITIM | 371 | 376 | PF00017 | 0.303 |
LIG_UBA3_1 | 405 | 414 | PF00899 | 0.295 |
LIG_WRC_WIRS_1 | 428 | 433 | PF05994 | 0.308 |
MOD_CDK_SPK_2 | 32 | 37 | PF00069 | 0.411 |
MOD_CDK_SPK_2 | 466 | 471 | PF00069 | 0.476 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.395 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.552 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.366 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.418 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.650 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.343 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.238 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.741 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.562 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.420 |
MOD_CMANNOS | 482 | 485 | PF00535 | 0.584 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.477 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.282 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.617 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.479 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.450 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.319 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.308 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.628 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.528 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.516 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.490 |
MOD_N-GLC_2 | 10 | 12 | PF02516 | 0.341 |
MOD_N-GLC_2 | 410 | 412 | PF02516 | 0.417 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.533 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.453 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.430 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.417 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.293 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.295 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.620 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.517 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.383 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.414 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.274 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.598 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.276 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.401 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.411 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.364 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.196 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.308 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.571 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.651 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.621 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.402 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.590 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.409 |
MOD_Plk_2-3 | 19 | 25 | PF00069 | 0.504 |
MOD_Plk_2-3 | 391 | 397 | PF00069 | 0.350 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.464 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.366 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.417 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.417 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.296 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.507 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.559 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.417 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.594 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.470 |
MOD_SUMO_rev_2 | 13 | 20 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 143 | 148 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 362 | 372 | PF00179 | 0.308 |
TRG_DiLeu_BaEn_1 | 367 | 372 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_4 | 367 | 373 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_4 | 78 | 84 | PF01217 | 0.245 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.397 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 351 | 355 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3S9 | Leptomonas seymouri | 67% | 100% |
A0A0S4JII5 | Bodo saltans | 46% | 74% |
A0A1X0P8D4 | Trypanosomatidae | 52% | 100% |
A0A3S7XA60 | Leishmania donovani | 88% | 100% |
A0A422NB33 | Trypanosoma rangeli | 52% | 100% |
A4ICX2 | Leishmania infantum | 88% | 100% |
D0A2H6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ASD3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q263 | Leishmania major | 87% | 100% |
V5C004 | Trypanosoma cruzi | 51% | 100% |