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: 20 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H3F4
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 4 |
GO:0006520 | amino acid metabolic process | 3 | 4 |
GO:0006560 | proline metabolic process | 6 | 4 |
GO:0006561 | proline biosynthetic process | 7 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008652 | amino acid biosynthetic process | 4 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0009064 | glutamine family amino acid metabolic process | 5 | 4 |
GO:0009084 | glutamine family amino acid biosynthetic process | 6 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016053 | organic acid biosynthetic process | 4 | 4 |
GO:0018130 | heterocycle biosynthetic process | 4 | 4 |
GO:0019752 | carboxylic acid metabolic process | 5 | 4 |
GO:0043436 | oxoacid metabolic process | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044281 | small molecule metabolic process | 2 | 4 |
GO:0044283 | small molecule biosynthetic process | 3 | 4 |
GO:0046394 | carboxylic acid biosynthetic process | 5 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0055129 | L-proline biosynthetic process | 5 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
GO:1901605 | alpha-amino acid metabolic process | 4 | 4 |
GO:1901607 | alpha-amino acid biosynthetic process | 5 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016620 | oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor | 4 | 10 |
GO:0016903 | oxidoreductase activity, acting on the aldehyde or oxo group of donors | 3 | 10 |
GO:0004350 | glutamate-5-semialdehyde dehydrogenase activity | 5 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.426 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.429 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.625 |
DEG_SPOP_SBC_1 | 156 | 160 | PF00917 | 0.534 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.534 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.423 |
DOC_ANK_TNKS_1 | 286 | 293 | PF00023 | 0.514 |
DOC_CKS1_1 | 131 | 136 | PF01111 | 0.540 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.578 |
DOC_CYCLIN_yCln2_LP_2 | 255 | 261 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 343 | 349 | PF00134 | 0.414 |
DOC_MAPK_DCC_7 | 115 | 124 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 330 | 340 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 355 | 362 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 115 | 124 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 355 | 362 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 504 | 512 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 633 | 640 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.648 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.425 |
DOC_PP2B_PxIxI_1 | 357 | 363 | PF00149 | 0.419 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 419 | 427 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 504 | 512 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 610 | 617 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 649 | 655 | PF00244 | 0.352 |
LIG_APCC_ABBA_1 | 47 | 52 | PF00400 | 0.340 |
LIG_APCC_ABBA_1 | 496 | 501 | PF00400 | 0.560 |
LIG_BIR_III_2 | 308 | 312 | PF00653 | 0.576 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.408 |
LIG_Clathr_ClatBox_1 | 569 | 573 | PF01394 | 0.420 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.620 |
LIG_eIF4E_1 | 385 | 391 | PF01652 | 0.298 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.533 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.543 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.601 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.387 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.410 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.423 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.560 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.380 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.567 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.466 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.646 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.666 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.687 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.502 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.535 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.454 |
LIG_FXI_DFP_1 | 499 | 503 | PF00024 | 0.419 |
LIG_LIR_Gen_1 | 382 | 391 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 421 | 431 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 458 | 466 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 482 | 492 | PF02991 | 0.439 |
LIG_LIR_LC3C_4 | 643 | 648 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.485 |
LIG_Pex14_1 | 285 | 289 | PF04695 | 0.495 |
LIG_Pex14_2 | 571 | 575 | PF04695 | 0.426 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.413 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.548 |
LIG_SH2_GRB2like | 385 | 388 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.357 |
LIG_SH2_SRC | 289 | 292 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 465 | 468 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 594 | 597 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.432 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.536 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.666 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.401 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 432 | 437 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 599 | 606 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 494 | 501 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 532 | 541 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 634 | 639 | PF11976 | 0.453 |
LIG_SxIP_EBH_1 | 445 | 456 | PF03271 | 0.542 |
LIG_TRAF2_1 | 524 | 527 | PF00917 | 0.399 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.427 |
LIG_UBA3_1 | 255 | 263 | PF00899 | 0.495 |
LIG_WRC_WIRS_1 | 572 | 577 | PF05994 | 0.434 |
MOD_CDC14_SPxK_1 | 146 | 149 | PF00782 | 0.677 |
MOD_CDC14_SPxK_1 | 257 | 260 | PF00782 | 0.501 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.685 |
MOD_CDK_SPxK_1 | 143 | 149 | PF00069 | 0.684 |
MOD_CDK_SPxK_1 | 254 | 260 | PF00069 | 0.643 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.688 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.615 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.576 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.443 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.562 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.359 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.584 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.565 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.664 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.566 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.686 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.589 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.455 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.539 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.410 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.451 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.583 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.665 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.571 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.690 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.641 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.573 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.421 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.311 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.407 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.424 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.656 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.609 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.579 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.670 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.511 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.632 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.712 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.477 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.511 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.470 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.534 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.425 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.290 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.639 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.551 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.538 |
MOD_N-GLC_1 | 605 | 610 | PF02516 | 0.531 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.586 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.683 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.589 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.535 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.528 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.464 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.507 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.488 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.309 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.427 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.543 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.463 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.433 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.541 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.541 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.312 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.532 |
MOD_PKA_1 | 148 | 154 | PF00069 | 0.657 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.657 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.591 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.567 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.439 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.411 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.432 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.484 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.535 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.429 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.433 |
MOD_Plk_2-3 | 535 | 541 | PF00069 | 0.493 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.533 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.433 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.454 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.454 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.546 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.531 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.668 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.574 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.650 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.567 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.646 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.632 |
TRG_DiLeu_BaEn_4 | 540 | 546 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 450 | 455 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITL0 | Leishmania donovani | 28% | 100% |
A0A451EJJ7 | Leishmania donovani | 83% | 100% |
A4HRQ8 | Leishmania infantum | 82% | 100% |
A4I8D9 | Leishmania infantum | 28% | 100% |
E9ACD7 | Leishmania major | 82% | 100% |
E9AJM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9B397 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q4V8 | Leishmania major | 28% | 100% |