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. | yes | yes: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACF1
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004617 | phosphoglycerate dehydrogenase activity | 5 | 6 |
GO:0005488 | binding | 1 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 8 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 8 |
GO:0016618 | hydroxypyruvate reductase activity | 5 | 2 |
GO:0030267 | glyoxylate reductase (NADP+) activity | 6 | 2 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0051287 | NAD binding | 4 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0106345 | glyoxylate reductase activity | 5 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 71 | 75 | PF00656 | 0.444 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.247 |
CLV_Separin_Metazoa | 430 | 434 | PF03568 | 0.410 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.447 |
DOC_CDC14_PxL_1 | 171 | 179 | PF14671 | 0.525 |
DOC_CDC14_PxL_1 | 281 | 289 | PF14671 | 0.563 |
DOC_CKS1_1 | 389 | 394 | PF01111 | 0.543 |
DOC_CYCLIN_RxL_1 | 123 | 131 | PF00134 | 0.526 |
DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 21 | 28 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.525 |
DOC_PP1_RVXF_1 | 90 | 96 | PF00149 | 0.452 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.448 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 161 | 170 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 226 | 235 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 495 | 505 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.453 |
LIG_Actin_WH2_2 | 340 | 357 | PF00022 | 0.563 |
LIG_Actin_WH2_2 | 487 | 504 | PF00022 | 0.579 |
LIG_APCC_ABBA_1 | 364 | 369 | PF00400 | 0.525 |
LIG_BIR_III_2 | 172 | 176 | PF00653 | 0.563 |
LIG_EH1_1 | 502 | 510 | PF00400 | 0.482 |
LIG_eIF4E_1 | 503 | 509 | PF01652 | 0.475 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.506 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.500 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.525 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.511 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.525 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.614 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.512 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.525 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.555 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.438 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.447 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.563 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.563 |
LIG_GBD_Chelix_1 | 460 | 468 | PF00786 | 0.337 |
LIG_Integrin_RGD_1 | 23 | 25 | PF01839 | 0.447 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.645 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.525 |
LIG_PTB_Apo_2 | 201 | 208 | PF02174 | 0.525 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.453 |
LIG_PTB_Phospho_1 | 72 | 78 | PF10480 | 0.451 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.416 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.421 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.525 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.525 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.499 |
LIG_SH3_CIN85_PxpxPR_1 | 140 | 145 | PF14604 | 0.447 |
LIG_SUMO_SIM_par_1 | 220 | 225 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 343 | 348 | PF11976 | 0.563 |
LIG_TYR_ITIM | 258 | 263 | PF00017 | 0.525 |
LIG_TYR_ITIM | 279 | 284 | PF00017 | 0.563 |
LIG_UBA3_1 | 221 | 227 | PF00899 | 0.508 |
LIG_UBA3_1 | 47 | 54 | PF00899 | 0.432 |
LIG_Vh1_VBS_1 | 336 | 354 | PF01044 | 0.563 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.614 |
LIG_WRC_WIRS_1 | 34 | 39 | PF05994 | 0.439 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.525 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.433 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.573 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.424 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.444 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.447 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.525 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.559 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.525 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.471 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.381 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.492 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.439 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.456 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.429 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.557 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.525 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.517 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.446 |
MOD_LATS_1 | 99 | 105 | PF00433 | 0.448 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.308 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.363 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.325 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.540 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.525 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.611 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.419 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.502 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.523 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.444 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.429 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.559 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.549 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.523 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.439 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.557 |
MOD_PKA_1 | 331 | 337 | PF00069 | 0.614 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.495 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.447 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.525 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.446 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.495 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.451 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.528 |
MOD_Plk_2-3 | 300 | 306 | PF00069 | 0.563 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.438 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.378 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.447 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.540 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.503 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.420 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.525 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.525 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.525 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 300 | 314 | PF08389 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRG6 | Leptomonas seymouri | 81% | 100% |
A0A1X0P8Z4 | Trypanosomatidae | 65% | 100% |
A0A2Z4HPZ6 | Hormonema carpetanum | 29% | 100% |
A0A3S5H520 | Leishmania donovani | 93% | 100% |
A4H3H6 | Leishmania braziliensis | 85% | 100% |
B3PK14 | Cellvibrio japonicus (strain Ueda107) | 27% | 100% |
E9AG23 | Leishmania infantum | 93% | 100% |
E9AJN9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O88712 | Mus musculus | 28% | 100% |
P0A9T0 | Escherichia coli (strain K12) | 52% | 100% |
P0A9T1 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 52% | 100% |
P0A9T2 | Escherichia coli O157:H7 | 52% | 100% |
P0A9T3 | Shigella flexneri | 52% | 100% |
P40054 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 49% | 100% |
P40510 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 100% |
P43885 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 49% | 100% |
P87228 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 49% | 100% |
Q13363 | Homo sapiens | 28% | 100% |
Q20595 | Caenorhabditis elegans | 26% | 70% |
Q54UH8 | Dictyostelium discoideum | 55% | 100% |
Q7N2B2 | Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01) | 26% | 100% |
Q9YHU0 | Xenopus laevis | 27% | 100% |
Q9Z2F5 | Rattus norvegicus | 28% | 100% |