Uncharacterized Protein, Mak10 subunit, NatC N(alpha)-terminal acetyltransferase
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. | yes | 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031248 | protein acetyltransferase complex | 3 | 12 |
GO:0031414 | N-terminal protein acetyltransferase complex | 4 | 12 |
GO:0031417 | NatC complex | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 12 |
GO:1902493 | acetyltransferase complex | 4 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WUK2
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 12 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 12 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018206 | peptidyl-methionine modification | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043543 | protein acylation | 5 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0051604 | protein maturation | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 576 | 580 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 732 | 734 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 734 | 736 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.516 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.490 |
DEG_APCC_DBOX_1 | 589 | 597 | PF00400 | 0.493 |
DEG_APCC_KENBOX_2 | 522 | 526 | PF00400 | 0.499 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.692 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.596 |
DEG_SPOP_SBC_1 | 188 | 192 | PF00917 | 0.540 |
DEG_SPOP_SBC_1 | 667 | 671 | PF00917 | 0.496 |
DOC_ANK_TNKS_1 | 681 | 688 | PF00023 | 0.601 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.662 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 166 | PF00134 | 0.681 |
DOC_CYCLIN_yCln2_LP_2 | 508 | 514 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 406 | 412 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 544 | 550 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 590 | 596 | PF00069 | 0.517 |
DOC_MAPK_RevD_3 | 418 | 433 | PF00069 | 0.470 |
DOC_MAPK_RevD_3 | 638 | 652 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 196 | 202 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.681 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.545 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.725 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.642 |
DOC_WD40_RPTOR_TOS_1 | 496 | 501 | PF00400 | 0.554 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 242 | 246 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 433 | 439 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 473 | 478 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 632 | 640 | PF00244 | 0.622 |
LIG_Actin_WH2_2 | 373 | 390 | PF00022 | 0.598 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.551 |
LIG_Clathr_ClatBox_1 | 296 | 300 | PF01394 | 0.573 |
LIG_Clathr_ClatBox_1 | 417 | 421 | PF01394 | 0.427 |
LIG_Clathr_ClatBox_1 | 604 | 608 | PF01394 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 13 | 22 | PF00928 | 0.541 |
LIG_eIF4E_1 | 582 | 588 | PF01652 | 0.540 |
LIG_eIF4E_1 | 66 | 72 | PF01652 | 0.530 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.542 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.544 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.612 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.508 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.634 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.528 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.647 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.451 |
LIG_FXI_DFP_1 | 113 | 117 | PF00024 | 0.547 |
LIG_LIR_Apic_2 | 337 | 343 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 158 | 168 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 413 | 424 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 440 | 449 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.542 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.551 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.478 |
LIG_Pex14_1 | 513 | 517 | PF04695 | 0.421 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.501 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.469 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.522 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.654 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.399 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.462 |
LIG_SH2_CRK | 619 | 623 | PF00017 | 0.601 |
LIG_SH2_GRB2like | 514 | 517 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 95 | 98 | PF00017 | 0.544 |
LIG_SH2_SRC | 95 | 98 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 630 | 634 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.449 |
LIG_SH3_2 | 317 | 322 | PF14604 | 0.428 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.711 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.520 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.454 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 230 | 237 | PF11976 | 0.511 |
LIG_SUMO_SIM_anti_2 | 499 | 504 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 475 | 482 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 592 | 598 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 603 | 608 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 88 | 94 | PF11976 | 0.434 |
LIG_SxIP_EBH_1 | 544 | 554 | PF03271 | 0.541 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.553 |
LIG_TRFH_1 | 161 | 165 | PF08558 | 0.657 |
LIG_TYR_ITIM | 617 | 622 | PF00017 | 0.594 |
LIG_UBA3_1 | 286 | 294 | PF00899 | 0.441 |
LIG_UBA3_1 | 593 | 601 | PF00899 | 0.500 |
LIG_WRC_WIRS_1 | 290 | 295 | PF05994 | 0.558 |
LIG_WRC_WIRS_1 | 493 | 498 | PF05994 | 0.463 |
MOD_CDK_SPxK_1 | 263 | 269 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 387 | 394 | PF00069 | 0.560 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.534 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.505 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.559 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.462 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.475 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.470 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.544 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.500 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.505 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.526 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.538 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.522 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.427 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.490 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.620 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.545 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.496 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.508 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.502 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.556 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.668 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.651 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.609 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.465 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.582 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.467 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.516 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.486 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.492 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.514 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.578 |
MOD_LATS_1 | 97 | 103 | PF00433 | 0.547 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.615 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.512 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.629 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.603 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.463 |
MOD_N-GLC_2 | 23 | 25 | PF02516 | 0.473 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.466 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.596 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.509 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.490 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.486 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.457 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.491 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.591 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.450 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.561 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.462 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.529 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.558 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.442 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.590 |
MOD_PKA_1 | 735 | 741 | PF00069 | 0.630 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.513 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.368 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.531 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.609 |
MOD_PKB_1 | 733 | 741 | PF00069 | 0.608 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.555 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.635 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.503 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.601 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.443 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.574 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.569 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.542 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.560 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.468 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.628 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.515 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.514 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.509 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.485 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.511 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.553 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.558 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.509 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.557 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.509 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.534 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.541 |
MOD_SUMO_for_1 | 26 | 29 | PF00179 | 0.623 |
MOD_SUMO_for_1 | 72 | 75 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 243 | 253 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 47 | 56 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 584 | 593 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.666 |
TRG_DiLeu_BaEn_1 | 230 | 235 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_1 | 589 | 594 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_4 | 63 | 69 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 611 | 616 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 681 | 683 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 732 | 735 | PF00400 | 0.635 |
TRG_NES_CRM1_1 | 230 | 245 | PF08389 | 0.465 |
TRG_NES_CRM1_1 | 288 | 300 | PF08389 | 0.566 |
TRG_NES_CRM1_1 | 491 | 505 | PF08389 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y3 | Leptomonas seymouri | 80% | 100% |
A0A0S4IMZ6 | Bodo saltans | 32% | 100% |
A0A1X0NSS7 | Trypanosomatidae | 52% | 100% |
A0A3R7M3C6 | Trypanosoma rangeli | 50% | 100% |
A4H953 | Leishmania braziliensis | 91% | 100% |
A4HXH5 | Leishmania infantum | 100% | 100% |
C9ZP62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AR70 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QE93 | Leishmania major | 98% | 100% |
V5D6H5 | Trypanosoma cruzi | 48% | 100% |