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: 5 |
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: E9AJM5
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006520 | amino acid metabolic process | 3 | 1 |
GO:0006560 | proline metabolic process | 6 | 1 |
GO:0006561 | proline biosynthetic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008652 | amino acid biosynthetic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009064 | glutamine family amino acid metabolic process | 5 | 1 |
GO:0009084 | glutamine family amino acid biosynthetic process | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016053 | organic acid biosynthetic process | 4 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0055129 | L-proline biosynthetic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 1 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0016620 | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor | 4 | 7 |
GO:0016903 | oxidoreductase activity, acting on the aldehyde or oxo group of donors | 3 | 7 |
GO:0004350 | glutamate-5-semialdehyde dehydrogenase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.531 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.366 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.457 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.660 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.532 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.433 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 255 | 261 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 343 | 349 | PF00134 | 0.427 |
DOC_MAPK_gen_1 | 330 | 340 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 355 | 362 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 36 | 43 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 355 | 362 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 504 | 512 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 633 | 640 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.651 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.436 |
DOC_PP2B_PxIxI_1 | 357 | 363 | PF00149 | 0.430 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.594 |
DOC_USP7_MATH_2 | 289 | 295 | PF00917 | 0.492 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 217 | 226 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 333 | 341 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 395 | 405 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 448 | 455 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 504 | 512 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 610 | 617 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.465 |
LIG_APCC_ABBA_1 | 496 | 501 | PF00400 | 0.559 |
LIG_BIR_III_4 | 118 | 122 | PF00653 | 0.671 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.426 |
LIG_Clathr_ClatBox_1 | 569 | 573 | PF01394 | 0.438 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.651 |
LIG_eIF4E_1 | 385 | 391 | PF01652 | 0.302 |
LIG_eIF4E_1 | 449 | 455 | PF01652 | 0.395 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.603 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.579 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.400 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.420 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.439 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.559 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.380 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.574 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.522 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.651 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.711 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.501 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.550 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.394 |
LIG_FXI_DFP_1 | 499 | 503 | PF00024 | 0.435 |
LIG_LIR_Gen_1 | 382 | 391 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 421 | 431 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 458 | 466 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 482 | 492 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.500 |
LIG_MYND_1 | 107 | 111 | PF01753 | 0.527 |
LIG_Pex14_1 | 101 | 105 | PF04695 | 0.537 |
LIG_Pex14_2 | 571 | 575 | PF04695 | 0.440 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.425 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.404 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.551 |
LIG_SH2_GRB2like | 385 | 388 | PF00017 | 0.313 |
LIG_SH2_NCK_1 | 449 | 453 | PF00017 | 0.404 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.369 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 465 | 468 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.449 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.658 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.658 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.416 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 432 | 437 | PF11976 | 0.428 |
LIG_SUMO_SIM_anti_2 | 599 | 606 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 38 | 46 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 494 | 501 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 634 | 639 | PF11976 | 0.470 |
LIG_SxIP_EBH_1 | 445 | 456 | PF03271 | 0.546 |
LIG_TRAF2_1 | 524 | 527 | PF00917 | 0.421 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.450 |
LIG_UBA3_1 | 255 | 263 | PF00899 | 0.509 |
LIG_WRC_WIRS_1 | 572 | 577 | PF05994 | 0.444 |
LIG_WW_2 | 316 | 319 | PF00397 | 0.532 |
MOD_CDC14_SPxK_1 | 146 | 149 | PF00782 | 0.719 |
MOD_CDC14_SPxK_1 | 257 | 260 | PF00782 | 0.517 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.717 |
MOD_CDK_SPxK_1 | 143 | 149 | PF00069 | 0.719 |
MOD_CDK_SPxK_1 | 254 | 260 | PF00069 | 0.641 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.719 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.764 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.604 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.645 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.458 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.547 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.513 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.708 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.583 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.462 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.551 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.435 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.465 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.697 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.740 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.586 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.609 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.706 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.589 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.426 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.425 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.496 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.487 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.699 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.690 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.741 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.805 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.516 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.643 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.498 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.515 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.391 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.488 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.541 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.443 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.287 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.646 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.601 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.541 |
MOD_N-GLC_1 | 605 | 610 | PF02516 | 0.584 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.724 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.611 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.482 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.509 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.487 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.423 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.374 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.434 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.326 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.531 |
MOD_NEK2_2 | 297 | 302 | PF00069 | 0.644 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.450 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.639 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.501 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.698 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.609 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.616 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.525 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.462 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.421 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.484 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.488 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.393 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.540 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.444 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.439 |
MOD_Plk_2-3 | 535 | 541 | PF00069 | 0.528 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.547 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.437 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.462 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.462 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.544 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.705 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.598 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.661 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.529 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.644 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.664 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.558 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.638 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.398 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.423 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.640 |
TRG_DiLeu_BaEn_1 | 515 | 520 | PF01217 | 0.399 |
TRG_DiLeu_BaEn_4 | 540 | 546 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A451EJJ7 | Leishmania donovani | 93% | 100% |
A4H3F4 | Leishmania braziliensis | 81% | 100% |
A4HRQ8 | Leishmania infantum | 92% | 100% |
E9ACD7 | Leishmania major | 92% | 100% |
E9B397 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |