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: A4H9T2
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 | 541 | 545 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.643 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 478 | 484 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.676 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.508 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 468 | 475 | PF00134 | 0.401 |
DOC_MAPK_gen_1 | 167 | 176 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 203 | 212 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 300 | 306 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 392 | 401 | PF00069 | 0.533 |
DOC_MAPK_HePTP_8 | 389 | 401 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 392 | 401 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 187 | 193 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.494 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.497 |
DOC_PP4_FxxP_1 | 323 | 326 | PF00568 | 0.506 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.687 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.566 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 10 | 18 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 144 | 148 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 288 | 294 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 460 | 466 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 482 | 492 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 528 | 538 | PF00244 | 0.302 |
LIG_Actin_WH2_2 | 551 | 569 | PF00022 | 0.306 |
LIG_APCC_ABBAyCdc20_2 | 556 | 562 | PF00400 | 0.417 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 295 | 299 | PF00928 | 0.525 |
LIG_eIF4E_1 | 505 | 511 | PF01652 | 0.627 |
LIG_eIF4E_1 | 99 | 105 | PF01652 | 0.632 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.494 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.537 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.558 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.384 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.398 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.548 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.610 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.466 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.605 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 311 | 317 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.545 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 487 | 493 | PF02991 | 0.700 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 378 | 389 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 431 | 441 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.417 |
LIG_MAD2 | 318 | 326 | PF02301 | 0.555 |
LIG_PDZ_Class_1 | 593 | 598 | PF00595 | 0.575 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.537 |
LIG_Pex14_1 | 492 | 496 | PF04695 | 0.590 |
LIG_Rb_LxCxE_1 | 396 | 414 | PF01857 | 0.301 |
LIG_RPA_C_Fungi | 5 | 17 | PF08784 | 0.629 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.403 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.399 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.425 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.665 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.626 |
LIG_SH2_GRB2like | 133 | 136 | PF00017 | 0.555 |
LIG_SH2_GRB2like | 35 | 38 | PF00017 | 0.636 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 35 | 39 | PF00017 | 0.665 |
LIG_SH2_SRC | 133 | 136 | PF00017 | 0.555 |
LIG_SH2_SRC | 35 | 38 | PF00017 | 0.666 |
LIG_SH2_STAP1 | 496 | 500 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.552 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.633 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 282 | 287 | PF11976 | 0.650 |
LIG_SUMO_SIM_anti_2 | 396 | 402 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 532 | 538 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 535 | 541 | PF11976 | 0.438 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.491 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.625 |
LIG_TRFH_1 | 152 | 156 | PF08558 | 0.448 |
LIG_TYR_ITSM | 250 | 257 | PF00017 | 0.445 |
MOD_CDK_SPK_2 | 313 | 318 | PF00069 | 0.542 |
MOD_CDK_SPK_2 | 411 | 416 | PF00069 | 0.326 |
MOD_CDK_SPxK_1 | 249 | 255 | PF00069 | 0.455 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.572 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.657 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.436 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.563 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.452 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.457 |
MOD_Cter_Amidation | 178 | 181 | PF01082 | 0.538 |
MOD_Cter_Amidation | 219 | 222 | PF01082 | 0.436 |
MOD_Cter_Amidation | 480 | 483 | PF01082 | 0.621 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.558 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.509 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.534 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.444 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.598 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.678 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.410 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.412 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.453 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.496 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.440 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.607 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.559 |
MOD_N-GLC_1 | 494 | 499 | PF02516 | 0.557 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.509 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.370 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.417 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.447 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.673 |
MOD_NEK2_2 | 576 | 581 | PF00069 | 0.547 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.569 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.572 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.586 |
MOD_PKA_1 | 180 | 186 | PF00069 | 0.625 |
MOD_PKA_1 | 287 | 293 | PF00069 | 0.585 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.526 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.625 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.574 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.529 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.604 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.553 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.635 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.386 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.578 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.596 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.645 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.398 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.344 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.339 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.707 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.423 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.579 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.543 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.450 |
MOD_SUMO_rev_2 | 166 | 171 | PF00179 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.704 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2F9 | Leptomonas seymouri | 80% | 100% |
A0A0S4IUG4 | Bodo saltans | 53% | 100% |
A0A1X0NVG4 | Trypanosomatidae | 66% | 97% |
A0A3S5H6I1 | Leishmania donovani | 91% | 100% |
A4HUT8 | Leishmania infantum | 91% | 100% |
D0A7M0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 99% |
E9ANH2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QH54 | Leishmania major | 91% | 100% |
V5BB32 | Trypanosoma cruzi | 65% | 100% |