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 |
Related structures:
AlphaFold database: Q4QH54
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 11 |
GO:0005996 | monosaccharide metabolic process | 3 | 11 |
GO:0006006 | glucose metabolic process | 5 | 11 |
GO:0006094 | gluconeogenesis | 6 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0016051 | carbohydrate biosynthetic process | 4 | 11 |
GO:0019318 | hexose metabolic process | 4 | 11 |
GO:0019319 | hexose biosynthetic process | 5 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0044283 | small molecule biosynthetic process | 3 | 11 |
GO:0046364 | monosaccharide biosynthetic process | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 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:0004611 | phosphoenolpyruvate carboxykinase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016829 | lyase activity | 2 | 11 |
GO:0016830 | carbon-carbon lyase activity | 3 | 11 |
GO:0016831 | carboxy-lyase activity | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.587 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 474 | 480 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.605 |
DOC_MAPK_gen_1 | 162 | 172 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 296 | 302 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 388 | 397 | PF00069 | 0.515 |
DOC_MAPK_HePTP_8 | 385 | 397 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.512 |
DOC_PP1_RVXF_1 | 183 | 189 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.467 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.537 |
DOC_PP4_FxxP_1 | 486 | 489 | PF00568 | 0.663 |
DOC_PP4_FxxP_1 | 507 | 510 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.586 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 140 | 144 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 478 | 488 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 581 | 588 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 6 | 16 | PF00244 | 0.629 |
LIG_APCC_ABBAyCdc20_2 | 552 | 558 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.422 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.670 |
LIG_deltaCOP1_diTrp_1 | 291 | 295 | PF00928 | 0.501 |
LIG_eIF4E_1 | 501 | 507 | PF01652 | 0.642 |
LIG_eIF4E_1 | 95 | 101 | PF01652 | 0.582 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.496 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.533 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.336 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.369 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.510 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.600 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.686 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.569 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.489 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.563 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 307 | 313 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 317 | 322 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.233 |
LIG_LIR_Apic_2 | 483 | 489 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 427 | 437 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.363 |
LIG_MAD2 | 314 | 322 | PF02301 | 0.511 |
LIG_PDZ_Class_1 | 589 | 594 | PF00595 | 0.492 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.500 |
LIG_Pex14_1 | 488 | 492 | PF04695 | 0.637 |
LIG_RPA_C_Fungi | 1 | 13 | PF08784 | 0.570 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.369 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.615 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.333 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.389 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.567 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.525 |
LIG_SH2_GRB2like | 30 | 33 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 129 | 133 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 30 | 34 | PF00017 | 0.615 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.525 |
LIG_SH2_SRC | 30 | 33 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 556 | 560 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.419 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.395 |
LIG_SUMO_SIM_anti_2 | 278 | 283 | PF11976 | 0.640 |
LIG_SUMO_SIM_anti_2 | 392 | 398 | PF11976 | 0.461 |
LIG_SUMO_SIM_anti_2 | 529 | 534 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.383 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.457 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.564 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.517 |
LIG_TRFH_1 | 148 | 152 | PF08558 | 0.394 |
LIG_TYR_ITIM | 28 | 33 | PF00017 | 0.651 |
LIG_TYR_ITSM | 246 | 253 | PF00017 | 0.397 |
LIG_WRC_WIRS_1 | 268 | 273 | PF05994 | 0.538 |
MOD_CDK_SPK_2 | 309 | 314 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.405 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.551 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.400 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.502 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.423 |
MOD_Cter_Amidation | 160 | 163 | PF01082 | 0.407 |
MOD_Cter_Amidation | 174 | 177 | PF01082 | 0.484 |
MOD_Cter_Amidation | 215 | 218 | PF01082 | 0.405 |
MOD_Cter_Amidation | 476 | 479 | PF01082 | 0.515 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.516 |
MOD_GlcNHglycan | 210 | 214 | PF01048 | 0.494 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.565 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.360 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.362 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.453 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.496 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.446 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.569 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.534 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.550 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.637 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.468 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.323 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.452 |
MOD_NEK2_2 | 572 | 577 | PF00069 | 0.452 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.443 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.551 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.593 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.527 |
MOD_PKA_1 | 283 | 289 | PF00069 | 0.567 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.488 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.527 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.619 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.567 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.480 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.335 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.566 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.532 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.473 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.614 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.361 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.639 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.375 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.397 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.522 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.401 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.367 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.553 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.498 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.411 |
TRG_DiLeu_BaEn_4 | 82 | 88 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.620 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 524 | 529 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2F9 | Leptomonas seymouri | 82% | 99% |
A0A0S4IUG4 | Bodo saltans | 53% | 100% |
A0A1X0NVG4 | Trypanosomatidae | 63% | 97% |
A0A3S5H6I1 | Leishmania donovani | 97% | 100% |
A4H9T2 | Leishmania braziliensis | 91% | 99% |
A4HUT8 | Leishmania infantum | 98% | 100% |
D0A7M0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 98% |
E9ANH2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BB32 | Trypanosoma cruzi | 65% | 100% |