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: E9ARR5
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 | 223 | 227 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.698 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.317 |
CLV_PCSK_FUR_1 | 561 | 565 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.338 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.359 |
CLV_Separin_Metazoa | 664 | 668 | PF03568 | 0.520 |
DEG_COP1_1 | 583 | 593 | PF00400 | 0.627 |
DEG_SCF_TRCP1_1 | 572 | 577 | PF00400 | 0.628 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.653 |
DOC_CDC14_PxL_1 | 381 | 389 | PF14671 | 0.592 |
DOC_CKS1_1 | 590 | 595 | PF01111 | 0.776 |
DOC_MAPK_gen_1 | 301 | 307 | PF00069 | 0.556 |
DOC_MAPK_RevD_3 | 191 | 207 | PF00069 | 0.520 |
DOC_MAPK_RevD_3 | 548 | 564 | PF00069 | 0.683 |
DOC_PP1_RVXF_1 | 657 | 663 | PF00149 | 0.641 |
DOC_PP1_RVXF_1 | 79 | 85 | PF00149 | 0.533 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.691 |
DOC_SPAK_OSR1_1 | 438 | 442 | PF12202 | 0.545 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.680 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 644 | 649 | PF00244 | 0.700 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BIR_III_2 | 100 | 104 | PF00653 | 0.511 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.613 |
LIG_deltaCOP1_diTrp_1 | 134 | 139 | PF00928 | 0.553 |
LIG_eIF4E_1 | 299 | 305 | PF01652 | 0.565 |
LIG_EVH1_1 | 550 | 554 | PF00568 | 0.665 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.734 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.467 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.487 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.569 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.537 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.681 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.662 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.633 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.482 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.623 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.695 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.639 |
LIG_LIR_Apic_2 | 616 | 622 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 483 | 493 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.464 |
LIG_MYND_1 | 548 | 552 | PF01753 | 0.626 |
LIG_NRBOX | 303 | 309 | PF00104 | 0.591 |
LIG_PCNA_yPIPBox_3 | 437 | 449 | PF02747 | 0.529 |
LIG_RPA_C_Fungi | 240 | 252 | PF08784 | 0.334 |
LIG_RPA_C_Fungi | 461 | 473 | PF08784 | 0.371 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.425 |
LIG_SH2_CRK | 687 | 691 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 111 | 115 | PF00017 | 0.318 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.441 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.518 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.324 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.432 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.684 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.612 |
LIG_SUMO_SIM_par_1 | 122 | 128 | PF11976 | 0.275 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.334 |
LIG_TRAF2_1 | 186 | 189 | PF00917 | 0.453 |
LIG_TRAF2_1 | 406 | 409 | PF00917 | 0.414 |
LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.494 |
LIG_TRAF2_1 | 533 | 536 | PF00917 | 0.608 |
LIG_TYR_ITIM | 685 | 690 | PF00017 | 0.334 |
LIG_WRC_WIRS_1 | 259 | 264 | PF05994 | 0.290 |
MOD_CDC14_SPxK_1 | 343 | 346 | PF00782 | 0.515 |
MOD_CDC14_SPxK_1 | 567 | 570 | PF00782 | 0.556 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.553 |
MOD_CDK_SPxK_1 | 340 | 346 | PF00069 | 0.516 |
MOD_CDK_SPxK_1 | 564 | 570 | PF00069 | 0.560 |
MOD_CDK_SPxK_1 | 604 | 610 | PF00069 | 0.616 |
MOD_CDK_SPxxK_3 | 340 | 347 | PF00069 | 0.517 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.598 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.537 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.571 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.571 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.535 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.562 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.334 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.592 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.549 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.629 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.597 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.576 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.490 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.401 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.396 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.424 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.468 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.524 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.557 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.593 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.576 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.605 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.579 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.470 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.554 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.646 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.459 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.348 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.600 |
MOD_GlcNHglycan | 571 | 575 | PF01048 | 0.583 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.552 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.339 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.503 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.573 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.577 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.624 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.507 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.576 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.741 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.530 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.625 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.610 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.532 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.279 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.623 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.520 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.641 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.567 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.343 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.602 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.481 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.334 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.645 |
MOD_PKA_1 | 644 | 650 | PF00069 | 0.602 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.486 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.453 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.684 |
MOD_Plk_2-3 | 386 | 392 | PF00069 | 0.424 |
MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.507 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.401 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.360 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.572 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.381 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.440 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.542 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.560 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.601 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.488 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.588 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.521 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.557 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.308 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.709 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.519 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.530 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.560 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.756 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.597 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 210 | 219 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 516 | 524 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 642 | 652 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_2 | 434 | 440 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 643 | 646 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.321 |
TRG_NLS_Bipartite_1 | 301 | 319 | PF00514 | 0.423 |
TRG_NLS_MonoCore_2 | 313 | 318 | PF00514 | 0.458 |
TRG_NLS_MonoExtN_4 | 314 | 319 | PF00514 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M7 | Leptomonas seymouri | 44% | 84% |
A0A3S7WV24 | Leishmania donovani | 86% | 99% |
A4H9N7 | Leishmania braziliensis | 66% | 98% |
A4HY02 | Leishmania infantum | 86% | 86% |
Q4QDQ8 | Leishmania major | 85% | 100% |