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: A0A3S7WT63
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_C14_Caspase3-7 | 531 | 535 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.662 |
CLV_PCSK_FUR_1 | 461 | 465 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.550 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.571 |
DEG_ODPH_VHL_1 | 98 | 110 | PF01847 | 0.443 |
DEG_SPOP_SBC_1 | 482 | 486 | PF00917 | 0.618 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.543 |
DOC_CKS1_1 | 80 | 85 | PF01111 | 0.645 |
DOC_CYCLIN_RxL_1 | 49 | 59 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 567 | 577 | PF00134 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 501 | 507 | PF00134 | 0.536 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.595 |
DOC_MAPK_FxFP_2 | 89 | 92 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 163 | 172 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 512 | 518 | PF00149 | 0.579 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.634 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.440 |
DOC_USP7_UBL2_3 | 487 | 491 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 416 | 422 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 488 | 494 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 553 | 561 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 72 | 80 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 547 | 564 | PF00022 | 0.580 |
LIG_APCC_ABBAyCdc20_2 | 52 | 58 | PF00400 | 0.537 |
LIG_BIR_III_2 | 534 | 538 | PF00653 | 0.607 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.542 |
LIG_eIF4E_1 | 2 | 8 | PF01652 | 0.540 |
LIG_eIF4E_1 | 349 | 355 | PF01652 | 0.453 |
LIG_EVH1_2 | 85 | 89 | PF00568 | 0.519 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.513 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.563 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.551 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.636 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.579 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.376 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.478 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.606 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.496 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.712 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.389 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.500 |
LIG_HCF-1_HBM_1 | 39 | 42 | PF13415 | 0.483 |
LIG_LIR_Apic_2 | 360 | 366 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 426 | 434 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 426 | 430 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 471 | 476 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 566 | 572 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.502 |
LIG_MYND_1 | 537 | 541 | PF01753 | 0.615 |
LIG_MYND_1 | 96 | 100 | PF01753 | 0.591 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.497 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.413 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.634 |
LIG_SH2_NCK_1 | 555 | 559 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 555 | 559 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.705 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.797 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.688 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.589 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.672 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.596 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.624 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.581 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.770 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.434 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.559 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.649 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.584 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.522 |
LIG_WW_2 | 313 | 316 | PF00397 | 0.649 |
LIG_WW_2 | 392 | 395 | PF00397 | 0.618 |
LIG_WW_2 | 537 | 540 | PF00397 | 0.618 |
LIG_WW_3 | 405 | 409 | PF00397 | 0.677 |
MOD_CDC14_SPxK_1 | 308 | 311 | PF00782 | 0.613 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.637 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.526 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.492 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.575 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.609 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.606 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.636 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.629 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.737 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.555 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.479 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.372 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.665 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.624 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.500 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.716 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.459 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.499 |
MOD_CMANNOS | 517 | 520 | PF00535 | 0.521 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.574 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.438 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.547 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.677 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.653 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.621 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.616 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.613 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.598 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.523 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.634 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.623 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.736 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.732 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.505 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.592 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.393 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.598 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.529 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.471 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.539 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.538 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.484 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.557 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.690 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.617 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.672 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.713 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.577 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.620 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.420 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.589 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.388 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.656 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.622 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.673 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.510 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.644 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.399 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.547 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.637 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.591 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.621 |
TRG_DiLeu_BaEn_4 | 444 | 450 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 119 | 124 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.634 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 35 | 39 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F8 | Leptomonas seymouri | 40% | 100% |
A4H7U8 | Leishmania braziliensis | 70% | 98% |
A4HW74 | Leishmania infantum | 100% | 100% |
E9APX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QFK6 | Leishmania major | 90% | 100% |