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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H7U8
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 7 |
GO:0006520 | amino acid metabolic process | 3 | 7 |
GO:0006560 | proline metabolic process | 6 | 7 |
GO:0006561 | proline biosynthetic process | 7 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008652 | amino acid biosynthetic process | 4 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009064 | glutamine family amino acid metabolic process | 5 | 7 |
GO:0009084 | glutamine family amino acid biosynthetic process | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016053 | organic acid biosynthetic process | 4 | 7 |
GO:0019752 | carboxylic acid metabolic process | 5 | 7 |
GO:0043436 | oxoacid metabolic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0044283 | small molecule biosynthetic process | 3 | 7 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 7 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 7 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0055129 | L-proline biosynthetic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004735 | pyrroline-5-carboxylate reductase activity | 5 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0016645 | oxidoreductase activity, acting on the CH-NH group of donors | 3 | 7 |
GO:0016646 | oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.783 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.488 |
CLV_Separin_Metazoa | 201 | 205 | PF03568 | 0.421 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.479 |
DOC_CDC14_PxL_1 | 273 | 281 | PF14671 | 0.473 |
DOC_CKS1_1 | 80 | 85 | PF01111 | 0.707 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 496 | 502 | PF00134 | 0.558 |
DOC_MAPK_DCC_7 | 312 | 320 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 108 | 115 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 312 | 320 | PF00069 | 0.528 |
DOC_MAPK_NFAT4_5 | 108 | 116 | PF00069 | 0.354 |
DOC_PP1_RVXF_1 | 507 | 513 | PF00149 | 0.624 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.659 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 224 | 234 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 245 | 250 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 341 | 346 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 485 | 489 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 548 | 556 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.550 |
LIG_Actin_WH2_2 | 542 | 559 | PF00022 | 0.616 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.421 |
LIG_APCC_ABBAyCdc20_2 | 52 | 58 | PF00400 | 0.592 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.555 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.530 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.476 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.610 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.584 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.624 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.541 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.614 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.559 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.721 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.411 |
LIG_HCF-1_HBM_1 | 39 | 42 | PF13415 | 0.530 |
LIG_LIR_Apic_2 | 136 | 142 | PF02991 | 0.236 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 383 | 388 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 3 | 13 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 422 | 430 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.393 |
LIG_MYND_1 | 101 | 105 | PF01753 | 0.623 |
LIG_MYND_1 | 86 | 90 | PF01753 | 0.520 |
LIG_PCNA_PIPBox_1 | 200 | 209 | PF02747 | 0.421 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.549 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.612 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 550 | 554 | PF00017 | 0.625 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 5 | 9 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 550 | 554 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.622 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.682 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.610 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.649 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.705 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.537 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.654 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.626 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 247 | 252 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.533 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.582 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.575 |
LIG_TYR_ITIM | 421 | 426 | PF00017 | 0.473 |
LIG_WRC_WIRS_1 | 279 | 284 | PF05994 | 0.593 |
LIG_WW_2 | 314 | 317 | PF00397 | 0.670 |
LIG_WW_3 | 401 | 405 | PF00397 | 0.700 |
MOD_CDK_SPxK_1 | 320 | 326 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 138 | 145 | PF00069 | 0.421 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.497 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.473 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.575 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.596 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.671 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.673 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.648 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.494 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.549 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.406 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.544 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.670 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.506 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.563 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.730 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.417 |
MOD_CMANNOS | 512 | 515 | PF00535 | 0.545 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.602 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.436 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.561 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.582 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.639 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.612 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.611 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.630 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.470 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.551 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.541 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.624 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.386 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.463 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.783 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.695 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.523 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.683 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.609 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.460 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.397 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.546 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.537 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.544 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.551 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.512 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.528 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.380 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.380 |
MOD_PKA_1 | 457 | 463 | PF00069 | 0.595 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.380 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.541 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.694 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.682 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.647 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.527 |
MOD_PKB_1 | 457 | 465 | PF00069 | 0.539 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.617 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.448 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.528 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.397 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.369 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.453 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.648 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.462 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.605 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.389 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.693 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.513 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.421 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.589 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.640 |
TRG_DiLeu_BaEn_4 | 440 | 446 | PF01217 | 0.605 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.640 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.696 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 35 | 39 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.548 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F8 | Leptomonas seymouri | 40% | 99% |
A0A3S7WT63 | Leishmania donovani | 70% | 99% |
A4HW74 | Leishmania infantum | 69% | 99% |
E9APX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
Q4QFK6 | Leishmania major | 71% | 99% |