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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQ61
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0003973 | (S)-2-hydroxy-acid oxidase activity | 5 | 1 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 2 |
GO:0016899 | oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor | 4 | 1 |
GO:0047545 | 2-hydroxyglutarate dehydrogenase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.262 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.286 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.272 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.272 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.173 |
DEG_SCF_FBW7_1 | 311 | 316 | PF00400 | 0.173 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.330 |
DOC_CYCLIN_RxL_1 | 293 | 303 | PF00134 | 0.173 |
DOC_MAPK_gen_1 | 330 | 337 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 346 | 353 | PF00069 | 0.254 |
DOC_MAPK_gen_1 | 53 | 61 | PF00069 | 0.398 |
DOC_MAPK_JIP1_4 | 488 | 494 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.276 |
DOC_MAPK_RevD_3 | 333 | 347 | PF00069 | 0.254 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.386 |
DOC_PP4_FxxP_1 | 451 | 454 | PF00568 | 0.374 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.173 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.246 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.326 |
DOC_USP7_UBL2_3 | 78 | 82 | PF12436 | 0.333 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.272 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.327 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 407 | 417 | PF00244 | 0.177 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.399 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_CSL_BTD_1 | 194 | 197 | PF09270 | 0.333 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.305 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.304 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.174 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.298 |
LIG_LIR_Apic_2 | 450 | 454 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.200 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.286 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.254 |
LIG_Pex14_2 | 377 | 381 | PF04695 | 0.351 |
LIG_Rb_pABgroove_1 | 155 | 163 | PF01858 | 0.386 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.254 |
LIG_SUMO_SIM_anti_2 | 247 | 254 | PF11976 | 0.173 |
LIG_SUMO_SIM_anti_2 | 58 | 63 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 369 | 374 | PF11976 | 0.173 |
LIG_SUMO_SIM_par_1 | 83 | 88 | PF11976 | 0.272 |
LIG_TRFH_1 | 309 | 313 | PF08558 | 0.293 |
LIG_UBA3_1 | 416 | 423 | PF00899 | 0.381 |
LIG_WRC_WIRS_1 | 426 | 431 | PF05994 | 0.268 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.492 |
MOD_CDK_SPxK_1 | 309 | 315 | PF00069 | 0.330 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.254 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.254 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.428 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.324 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.184 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.342 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.331 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.272 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.258 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.318 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.345 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.271 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.463 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.278 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.297 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.548 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.425 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.518 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.286 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.333 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.331 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.230 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.497 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.405 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.311 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.254 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.173 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.323 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.386 |
MOD_PK_1 | 331 | 337 | PF00069 | 0.272 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.468 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.298 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.300 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.333 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.381 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.452 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.254 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.305 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.330 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.265 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.272 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.325 |
MOD_SUMO_rev_2 | 419 | 425 | PF00179 | 0.381 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_1 | 314 | 319 | PF01217 | 0.190 |
TRG_DiLeu_BaEn_1 | 412 | 417 | PF01217 | 0.249 |
TRG_DiLeu_BaLyEn_6 | 294 | 299 | PF01217 | 0.173 |
TRG_DiLeu_BaLyEn_6 | 486 | 491 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.409 |
TRG_NES_CRM1_1 | 424 | 439 | PF08389 | 0.268 |
TRG_NLS_MonoExtC_3 | 75 | 80 | PF00514 | 0.173 |
TRG_NLS_MonoExtN_4 | 28 | 33 | PF00514 | 0.328 |
TRG_NLS_MonoExtN_4 | 73 | 80 | PF00514 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.173 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.268 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1P3 | Leptomonas seymouri | 23% | 100% |
A0A0N1PEN9 | Leptomonas seymouri | 76% | 100% |
A0A0S4JUB7 | Bodo saltans | 42% | 100% |
A0A1X0P066 | Trypanosomatidae | 58% | 100% |
A0A3Q8IJT1 | Leishmania donovani | 86% | 100% |
A0A5Y6MCT2 | Salmonella houtenae | 31% | 100% |
A4IDW0 | Leishmania infantum | 86% | 100% |
A7MBI3 | Bos taurus | 32% | 100% |
A7SMW7 | Nematostella vectensis | 35% | 100% |
A8X2R1 | Caenorhabditis briggsae | 32% | 100% |
B7N6P4 | Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) | 31% | 100% |
D0A456 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9ATY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
P37339 | Escherichia coli (strain K12) | 31% | 100% |
Q4Q0L5 | Leishmania major | 85% | 100% |
Q55GI5 | Dictyostelium discoideum | 33% | 100% |
Q91YP0 | Mus musculus | 34% | 100% |
Q9H9P8 | Homo sapiens | 31% | 100% |
Q9LES4 | Arabidopsis thaliana | 25% | 100% |
Q9N4Z0 | Caenorhabditis elegans | 33% | 100% |
S2DJ52 | Indibacter alkaliphilus (strain CCUG 57479 / KCTC 22604 / LW1) | 30% | 100% |
V5DK53 | Trypanosoma cruzi | 57% | 100% |