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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
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: A4HF16
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 12 |
GO:0006520 | amino acid metabolic process | 3 | 12 |
GO:0006560 | proline metabolic process | 6 | 12 |
GO:0006562 | proline catabolic process | 5 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009063 | amino acid catabolic process | 4 | 12 |
GO:0009064 | glutamine family amino acid metabolic process | 5 | 12 |
GO:0009065 | glutamine family amino acid catabolic process | 6 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016054 | organic acid catabolic process | 4 | 12 |
GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
GO:0043436 | oxoacid metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0044282 | small molecule catabolic process | 3 | 12 |
GO:0046395 | carboxylic acid catabolic process | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 12 |
GO:1901606 | alpha-amino acid catabolic process | 5 | 12 |
GO:0006536 | glutamate metabolic process | 6 | 1 |
GO:0010133 | proline catabolic process to glutamate | 6 | 1 |
GO:0043648 | dicarboxylic acid metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004657 | proline dehydrogenase activity | 5 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016645 | oxidoreductase activity, acting on the CH-NH group of donors | 3 | 12 |
GO:0016649 | oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor | 4 | 12 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 5 |
GO:0005509 | calcium ion binding | 5 | 5 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043168 | anion binding | 3 | 1 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 1 |
GO:0071949 | FAD binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 543 | 547 | PF00656 | 0.574 |
CLV_MEL_PAP_1 | 204 | 210 | PF00089 | 0.275 |
CLV_MEL_PAP_1 | 488 | 494 | PF00089 | 0.311 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.244 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.181 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 484 | 486 | PF00082 | 0.168 |
CLV_PCSK_PC1ET2_1 | 557 | 559 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.397 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.642 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 501 | 508 | PF00134 | 0.511 |
DOC_MAPK_gen_1 | 242 | 248 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 461 | 467 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 501 | 508 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 52 | 59 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 489 | 495 | PF00149 | 0.511 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.269 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.420 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 323 | 327 | PF12436 | 0.511 |
DOC_USP7_UBL2_3 | 553 | 557 | PF12436 | 0.378 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 207 | 215 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 332 | 336 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 421 | 429 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.412 |
LIG_Clathr_ClatBox_1 | 228 | 232 | PF01394 | 0.252 |
LIG_Clathr_ClatBox_1 | 299 | 303 | PF01394 | 0.511 |
LIG_EH1_1 | 48 | 56 | PF00400 | 0.378 |
LIG_eIF4E_1 | 49 | 55 | PF01652 | 0.374 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.500 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.463 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.511 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.473 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.476 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.409 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.402 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.537 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.377 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.390 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.433 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.410 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.521 |
LIG_LIR_Gen_1 | 249 | 257 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 268 | 278 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 249 | 253 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.329 |
LIG_Pex14_1 | 219 | 223 | PF04695 | 0.302 |
LIG_Pex14_2 | 494 | 498 | PF04695 | 0.511 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.397 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.395 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.409 |
LIG_SH2_CRK | 516 | 520 | PF00017 | 0.423 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.395 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.340 |
LIG_SH2_NCK_1 | 260 | 264 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 444 | 448 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 86 | 90 | PF00017 | 0.414 |
LIG_SH2_STAT3 | 416 | 419 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.384 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.632 |
LIG_SH3_1 | 517 | 523 | PF00018 | 0.409 |
LIG_SH3_2 | 520 | 525 | PF14604 | 0.409 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.427 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.598 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 473 | 479 | PF11976 | 0.511 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 298 | 303 | PF11976 | 0.438 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.400 |
LIG_TRAF2_1 | 436 | 439 | PF00917 | 0.420 |
LIG_TRFH_1 | 5 | 9 | PF08558 | 0.405 |
LIG_TYR_ITIM | 248 | 253 | PF00017 | 0.407 |
LIG_TYR_ITIM | 519 | 524 | PF00017 | 0.409 |
LIG_TYR_ITIM | 84 | 89 | PF00017 | 0.342 |
LIG_WRC_WIRS_1 | 452 | 457 | PF05994 | 0.463 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.432 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.395 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.521 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.509 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.573 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.498 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.536 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.349 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.416 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.317 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.433 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.411 |
MOD_Cter_Amidation | 531 | 534 | PF01082 | 0.209 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.626 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.286 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.263 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.360 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.442 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.546 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.444 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.457 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.305 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.251 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.233 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.393 |
MOD_N-GLC_2 | 441 | 443 | PF02516 | 0.276 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.362 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.365 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.431 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.433 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.463 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.463 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.409 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.420 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.355 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.534 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.492 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.710 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.274 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.432 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.433 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.245 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.450 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.363 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.409 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.389 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.441 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.419 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.365 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.385 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.444 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.405 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.402 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.281 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.511 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.432 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.385 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.409 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.370 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.509 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.433 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.409 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.454 |
MOD_SUMO_for_1 | 229 | 232 | PF00179 | 0.469 |
MOD_SUMO_for_1 | 552 | 555 | PF00179 | 0.288 |
TRG_DiLeu_BaEn_4 | 226 | 232 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.473 |
TRG_NLS_MonoExtN_4 | 554 | 561 | PF00514 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.220 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUG0 | Leptomonas seymouri | 77% | 99% |
A0A0S4JS18 | Bodo saltans | 39% | 99% |
A0A1X0NS42 | Trypanosomatidae | 57% | 100% |
A0A3Q8IFX0 | Leishmania donovani | 93% | 100% |
A0A3R7N3G7 | Trypanosoma rangeli | 54% | 100% |
A4I294 | Leishmania infantum | 92% | 100% |
C9ZRP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AYE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O43272 | Homo sapiens | 30% | 94% |
O45228 | Caenorhabditis elegans | 29% | 91% |
Q04499 | Drosophila melanogaster | 30% | 83% |
Q148G5 | Bos taurus | 28% | 95% |
Q4Q933 | Leishmania major | 92% | 100% |
Q9WU79 | Mus musculus | 30% | 94% |
V5B5Q5 | Trypanosoma cruzi | 56% | 99% |