Amino acid metabolism, Proline oxidase, mitochondrial-like
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I294
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 | 390 | 394 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.553 |
CLV_MEL_PAP_1 | 203 | 209 | PF00089 | 0.284 |
CLV_MEL_PAP_1 | 487 | 493 | PF00089 | 0.287 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.201 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.201 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.262 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.369 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.621 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 500 | 507 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 241 | 247 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 460 | 466 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 500 | 507 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 51 | 58 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 488 | 494 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.413 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 322 | 326 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 206 | 214 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 331 | 335 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 420 | 428 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.479 |
LIG_Clathr_ClatBox_1 | 298 | 302 | PF01394 | 0.487 |
LIG_EH1_1 | 47 | 55 | PF00400 | 0.451 |
LIG_eIF4E_1 | 48 | 54 | PF01652 | 0.447 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.499 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.442 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.487 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.442 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.401 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.493 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.495 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.415 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.402 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.580 |
LIG_LIR_Gen_1 | 248 | 256 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 60 | 71 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.321 |
LIG_Pex14_1 | 218 | 222 | PF04695 | 0.322 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.487 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.382 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.400 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.401 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.416 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.386 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 415 | 418 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.371 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.615 |
LIG_SH3_1 | 428 | 434 | PF00018 | 0.362 |
LIG_SH3_1 | 516 | 522 | PF00018 | 0.401 |
LIG_SH3_2 | 519 | 524 | PF14604 | 0.401 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.521 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.475 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.615 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.360 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.396 |
LIG_SH3_4 | 153 | 160 | PF00018 | 0.445 |
LIG_SUMO_SIM_anti_2 | 472 | 478 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 297 | 302 | PF11976 | 0.431 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.421 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.413 |
LIG_TYR_ITIM | 247 | 252 | PF00017 | 0.409 |
LIG_TYR_ITIM | 518 | 523 | PF00017 | 0.401 |
LIG_TYR_ITIM | 83 | 88 | PF00017 | 0.339 |
LIG_UBA3_1 | 334 | 340 | PF00899 | 0.444 |
LIG_UBA3_1 | 551 | 556 | PF00899 | 0.465 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.506 |
MOD_CDK_SPK_2 | 180 | 185 | PF00069 | 0.503 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.382 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.488 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.464 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.548 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.448 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.493 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.408 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.415 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.394 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.462 |
MOD_Cter_Amidation | 530 | 533 | PF01082 | 0.201 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.595 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.291 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.306 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.444 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.585 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.325 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.365 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.395 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.412 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.515 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.504 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.403 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.431 |
MOD_N-GLC_1 | 501 | 506 | PF02516 | 0.242 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.226 |
MOD_N-GLC_1 | 545 | 550 | PF02516 | 0.393 |
MOD_N-GLC_2 | 440 | 442 | PF02516 | 0.262 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.367 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.588 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.351 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.409 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.506 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.506 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.401 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.431 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.413 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.597 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.498 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.471 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.664 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.284 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.398 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.426 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.481 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.362 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.480 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.401 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.361 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.433 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.413 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.365 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.385 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.435 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.398 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.393 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.478 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.421 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.386 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.318 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.488 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.413 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.393 |
MOD_SUMO_for_1 | 228 | 231 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_4 | 225 | 231 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.448 |
TRG_NLS_MonoExtN_4 | 553 | 560 | PF00514 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.213 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUG0 | Leptomonas seymouri | 79% | 99% |
A0A0S4JS18 | Bodo saltans | 38% | 99% |
A0A1X0NS42 | Trypanosomatidae | 56% | 100% |
A0A3Q8IFX0 | Leishmania donovani | 100% | 100% |
A0A3R7N3G7 | Trypanosoma rangeli | 55% | 100% |
A4HF16 | Leishmania braziliensis | 92% | 100% |
C9ZRP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AYE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
O43272 | Homo sapiens | 30% | 94% |
O45228 | Caenorhabditis elegans | 30% | 91% |
Q04499 | Drosophila melanogaster | 30% | 82% |
Q148G5 | Bos taurus | 29% | 95% |
Q4Q933 | Leishmania major | 98% | 100% |
Q9WU79 | Mus musculus | 30% | 94% |
V5B5Q5 | Trypanosoma cruzi | 54% | 99% |