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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H9N7
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007059 | chromosome segregation | 2 | 5 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018206 | peptidyl-methionine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0043966 | histone H3 acetylation | 7 | 1 |
GO:0043967 | histone H4 acetylation | 7 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004596 | peptide alpha-N-acetyltransferase activity | 8 | 7 |
GO:0008080 | N-acetyltransferase activity | 6 | 7 |
GO:0016407 | acetyltransferase activity | 5 | 7 |
GO:0016410 | N-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 7 |
GO:0004402 | histone acetyltransferase activity | 4 | 1 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 182 | 186 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.291 |
CLV_PCSK_FUR_1 | 526 | 530 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.450 |
CLV_PCSK_PC7_1 | 392 | 398 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.396 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.599 |
DEG_SPOP_SBC_1 | 517 | 521 | PF00917 | 0.651 |
DOC_CKS1_1 | 560 | 565 | PF01111 | 0.683 |
DOC_MAPK_gen_1 | 533 | 540 | PF00069 | 0.623 |
DOC_MAPK_RevD_3 | 513 | 529 | PF00069 | 0.660 |
DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.552 |
DOC_PP1_RVXF_1 | 625 | 631 | PF00149 | 0.647 |
DOC_PP2B_LxvP_1 | 567 | 570 | PF13499 | 0.609 |
DOC_PP2B_PxIxI_1 | 505 | 511 | PF00149 | 0.622 |
DOC_SPAK_OSR1_1 | 397 | 401 | PF12202 | 0.548 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 41 | 56 | PF00022 | 0.465 |
LIG_APCC_ABBA_1 | 427 | 432 | PF00400 | 0.474 |
LIG_BIR_III_2 | 311 | 315 | PF00653 | 0.630 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.644 |
LIG_CaM_IQ_9 | 87 | 102 | PF13499 | 0.509 |
LIG_eIF4E_1 | 258 | 264 | PF01652 | 0.569 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.560 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.512 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.540 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.617 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.585 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.254 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.328 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.499 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.677 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.653 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.636 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.610 |
LIG_GBD_Chelix_1 | 192 | 200 | PF00786 | 0.236 |
LIG_LIR_Apic_2 | 585 | 590 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 592 | 596 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.477 |
LIG_LYPXL_yS_3 | 593 | 596 | PF13949 | 0.611 |
LIG_NRBOX | 262 | 268 | PF00104 | 0.599 |
LIG_PCNA_yPIPBox_3 | 394 | 408 | PF02747 | 0.540 |
LIG_RPA_C_Fungi | 199 | 211 | PF08784 | 0.472 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.334 |
LIG_SH2_NCK_1 | 545 | 549 | PF00017 | 0.498 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.318 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.511 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.495 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.373 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.727 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 84 | 90 | PF11976 | 0.278 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.457 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.364 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.557 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.520 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.322 |
LIG_TYR_ITIM | 653 | 658 | PF00017 | 0.334 |
LIG_WRC_WIRS_1 | 218 | 223 | PF05994 | 0.342 |
MOD_CDK_SPK_2 | 586 | 591 | PF00069 | 0.534 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.560 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.560 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.586 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.545 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.416 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.586 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.527 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.598 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.523 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.511 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.360 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.590 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.554 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.488 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.547 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.551 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.539 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.407 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.554 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.534 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.626 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.611 |
MOD_GlcNHglycan | 456 | 461 | PF01048 | 0.552 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.595 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.507 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.671 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.596 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.613 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.615 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.759 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.466 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.374 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.486 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.623 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.586 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.575 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.430 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.486 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.532 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.567 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.533 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.414 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.537 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.614 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.560 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.221 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.221 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.551 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.450 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.403 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.655 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.503 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.348 |
MOD_PKA_1 | 583 | 589 | PF00069 | 0.491 |
MOD_PKA_1 | 612 | 618 | PF00069 | 0.601 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.345 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.565 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.683 |
MOD_PKB_1 | 356 | 364 | PF00069 | 0.377 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.353 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.666 |
MOD_Plk_2-3 | 381 | 387 | PF00069 | 0.530 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.476 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.446 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.356 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.565 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.381 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.347 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.555 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.407 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.503 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.560 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.511 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.562 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.562 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.552 |
MOD_SUMO_rev_2 | 254 | 264 | PF00179 | 0.359 |
TRG_DiLeu_BaEn_4 | 609 | 615 | PF01217 | 0.469 |
TRG_DiLeu_LyEn_5 | 503 | 508 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.336 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 582 | 584 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.579 |
TRG_NLS_MonoExtC_3 | 392 | 397 | PF00514 | 0.405 |
TRG_NLS_MonoExtN_4 | 392 | 397 | PF00514 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M7 | Leptomonas seymouri | 43% | 80% |
A0A3S7WV24 | Leishmania donovani | 70% | 94% |
A4HY02 | Leishmania infantum | 70% | 82% |
E9ARR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 95% |
Q4QDQ8 | Leishmania major | 69% | 100% |