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: A0A3S7WV24
Term | Name | Level | Count |
---|---|---|---|
GO:0007059 | chromosome segregation | 2 | 6 |
GO:0009987 | cellular process | 1 | 6 |
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:0008152 | metabolic process | 1 | 1 |
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 | 224 | 228 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.712 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.331 |
CLV_PCSK_FUR_1 | 568 | 572 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 302 | 304 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.314 |
CLV_PCSK_PC7_1 | 435 | 441 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.335 |
DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.697 |
DEG_SPOP_SBC_1 | 41 | 45 | PF00917 | 0.661 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.688 |
DEG_SPOP_SBC_1 | 73 | 77 | PF00917 | 0.609 |
DOC_CDC14_PxL_1 | 383 | 391 | PF14671 | 0.609 |
DOC_CKS1_1 | 602 | 607 | PF01111 | 0.835 |
DOC_MAPK_gen_1 | 302 | 308 | PF00069 | 0.584 |
DOC_MAPK_RevD_3 | 555 | 571 | PF00069 | 0.681 |
DOC_PP1_RVXF_1 | 675 | 682 | PF00149 | 0.576 |
DOC_PP1_RVXF_1 | 80 | 86 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.692 |
DOC_SPAK_OSR1_1 | 440 | 444 | PF12202 | 0.562 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 345 | 350 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 654 | 659 | PF00244 | 0.677 |
LIG_BIR_III_2 | 101 | 105 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.659 |
LIG_CaM_IQ_9 | 126 | 141 | PF13499 | 0.528 |
LIG_deltaCOP1_diTrp_1 | 135 | 140 | PF00928 | 0.581 |
LIG_eIF4E_1 | 300 | 306 | PF01652 | 0.552 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.676 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.468 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.468 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.468 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.668 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.677 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.562 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.703 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.671 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.495 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.646 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.701 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.627 |
LIG_LIR_Apic_2 | 626 | 632 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 376 | 387 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 634 | 638 | PF02991 | 0.595 |
LIG_LYPXL_yS_3 | 635 | 638 | PF13949 | 0.599 |
LIG_NRBOX | 304 | 310 | PF00104 | 0.588 |
LIG_PCNA_yPIPBox_3 | 439 | 451 | PF02747 | 0.541 |
LIG_Rb_LxCxE_1 | 665 | 678 | PF01857 | 0.571 |
LIG_RPA_C_Fungi | 241 | 253 | PF08784 | 0.363 |
LIG_RPA_C_Fungi | 463 | 475 | PF08784 | 0.393 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.364 |
LIG_SH2_CRK | 697 | 701 | PF00017 | 0.363 |
LIG_SH2_SRC | 349 | 352 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 285 | 288 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.428 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.633 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.352 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.482 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.590 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.544 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.600 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.492 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.356 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.427 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.608 |
LIG_TRAF2_1 | 535 | 538 | PF00917 | 0.729 |
LIG_TYR_ITIM | 695 | 700 | PF00017 | 0.363 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.302 |
MOD_CDC14_SPxK_1 | 574 | 577 | PF00782 | 0.562 |
MOD_CDK_SPK_2 | 144 | 149 | PF00069 | 0.575 |
MOD_CDK_SPK_2 | 628 | 633 | PF00069 | 0.516 |
MOD_CDK_SPxK_1 | 571 | 577 | PF00069 | 0.562 |
MOD_CDK_SPxK_1 | 614 | 620 | PF00069 | 0.621 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.658 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.627 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.646 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.695 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.570 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.363 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.604 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.617 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.628 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.622 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.634 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.579 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.487 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.436 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.430 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.445 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.520 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.466 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.797 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.602 |
MOD_DYRK1A_RPxSP_1 | 571 | 575 | PF00069 | 0.538 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.640 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.631 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.486 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.595 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.649 |
MOD_GlcNHglycan | 499 | 503 | PF01048 | 0.562 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.615 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.597 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.613 |
MOD_GlcNHglycan | 610 | 614 | PF01048 | 0.641 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.720 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.587 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.618 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.562 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.654 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.714 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.662 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.507 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.476 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.652 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.697 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.701 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.635 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.668 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.575 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.564 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.493 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.317 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.658 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.539 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.675 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.613 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.506 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.588 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.470 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.633 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.363 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.686 |
MOD_PKA_1 | 654 | 660 | PF00069 | 0.642 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.514 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.519 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.683 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.435 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.442 |
MOD_Plk_2-3 | 424 | 430 | PF00069 | 0.466 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.475 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.393 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.465 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.374 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.579 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.477 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.464 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.344 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.504 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.703 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.582 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.643 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.532 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.747 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.562 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.749 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.597 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.446 |
MOD_SUMO_rev_2 | 652 | 662 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_2 | 436 | 442 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 653 | 656 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.336 |
TRG_NLS_Bipartite_1 | 302 | 320 | PF00514 | 0.408 |
TRG_NLS_MonoCore_2 | 314 | 319 | PF00514 | 0.456 |
TRG_NLS_MonoExtN_4 | 315 | 320 | PF00514 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M7 | Leptomonas seymouri | 45% | 85% |
A4H9N7 | Leishmania braziliensis | 70% | 100% |
A4HY02 | Leishmania infantum | 100% | 100% |
E9ARR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QDQ8 | Leishmania major | 89% | 100% |