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: 3 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9ANQ1
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 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:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016409 | palmitoyltransferase activity | 5 | 9 |
GO:0016417 | S-acyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 9 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.539 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 601 | 603 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 70 | 76 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.257 |
DEG_SCF_FBW7_1 | 11 | 17 | PF00400 | 0.651 |
DEG_SCF_FBW7_1 | 21 | 27 | PF00400 | 0.632 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.637 |
DOC_CKS1_1 | 11 | 16 | PF01111 | 0.656 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.634 |
DOC_MAPK_gen_1 | 601 | 608 | PF00069 | 0.595 |
DOC_MAPK_RevD_3 | 300 | 316 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 518 | 524 | PF00149 | 0.411 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.601 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.639 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.639 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.660 |
DOC_USP7_MATH_2 | 237 | 243 | PF00917 | 0.684 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.578 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.652 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 389 | 393 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 400 | 406 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 520 | 526 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 53 | 63 | PF00244 | 0.690 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.708 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.319 |
LIG_EH1_1 | 445 | 453 | PF00400 | 0.215 |
LIG_eIF4E_1 | 458 | 464 | PF01652 | 0.327 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.665 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.641 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.688 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.657 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.647 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.332 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.303 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.662 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.641 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 31 | 37 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 376 | 385 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 545 | 552 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 585 | 590 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 593 | 599 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 585 | 589 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 593 | 598 | PF02991 | 0.488 |
LIG_MLH1_MIPbox_1 | 555 | 559 | PF16413 | 0.319 |
LIG_PCNA_yPIPBox_3 | 436 | 444 | PF02747 | 0.379 |
LIG_Pex14_1 | 421 | 425 | PF04695 | 0.430 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.660 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.366 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.544 |
LIG_SH2_GRB2like | 472 | 475 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.615 |
LIG_SH2_PTP2 | 378 | 381 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 428 | 431 | PF00017 | 0.393 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.544 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.634 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.736 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.714 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.702 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.676 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.639 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.687 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.656 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.650 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.674 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.680 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.660 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.611 |
LIG_Sin3_3 | 447 | 454 | PF02671 | 0.303 |
LIG_SUMO_SIM_anti_2 | 413 | 418 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 459 | 465 | PF11976 | 0.363 |
LIG_SUMO_SIM_anti_2 | 568 | 573 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 459 | 465 | PF11976 | 0.363 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.681 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.617 |
LIG_TYR_ITSM | 591 | 598 | PF00017 | 0.541 |
LIG_UBA3_1 | 214 | 222 | PF00899 | 0.661 |
LIG_UBA3_1 | 461 | 467 | PF00899 | 0.448 |
LIG_WRC_WIRS_1 | 463 | 468 | PF05994 | 0.348 |
LIG_WRC_WIRS_1 | 522 | 527 | PF05994 | 0.473 |
LIG_WW_3 | 145 | 149 | PF00397 | 0.629 |
MOD_CDC14_SPxK_1 | 145 | 148 | PF00782 | 0.624 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.652 |
MOD_CDK_SPxK_1 | 142 | 148 | PF00069 | 0.630 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.651 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.644 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.630 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.706 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.705 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.726 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.665 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.486 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.657 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.670 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.678 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.663 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.670 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.752 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.696 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.645 |
MOD_Cter_Amidation | 363 | 366 | PF01082 | 0.402 |
MOD_Cter_Amidation | 43 | 46 | PF01082 | 0.456 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.505 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.480 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.502 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.456 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.470 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.429 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.319 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.430 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.519 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.443 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.489 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.664 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.640 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.731 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.683 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.619 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.702 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.631 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.650 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.667 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.564 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.676 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.647 |
MOD_LATS_1 | 73 | 79 | PF00433 | 0.655 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.403 |
MOD_N-GLC_2 | 497 | 499 | PF02516 | 0.364 |
MOD_N-GLC_2 | 511 | 513 | PF02516 | 0.364 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.691 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.727 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.629 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.508 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.395 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.335 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.387 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.615 |
MOD_NEK2_2 | 373 | 378 | PF00069 | 0.570 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.638 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.637 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.599 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.422 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.564 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.658 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.688 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.642 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.640 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.660 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.667 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.715 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.564 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.307 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.556 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.658 |
MOD_PKB_1 | 117 | 125 | PF00069 | 0.695 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.691 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.704 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.588 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.639 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.629 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.710 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.681 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.640 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.566 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.430 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.375 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.361 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.359 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.303 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.335 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.771 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.642 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.700 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.772 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.637 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.729 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 110 | 115 | PF00179 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 621 | 624 | PF00400 | 0.641 |
TRG_NLS_Bipartite_1 | 601 | 622 | PF00514 | 0.625 |
TRG_NLS_MonoExtC_3 | 617 | 622 | PF00514 | 0.610 |
TRG_NLS_MonoExtC_3 | 67 | 72 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 616 | 622 | PF00514 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WRS6 | Leishmania donovani | 86% | 100% |
A4H6N2 | Leishmania braziliensis | 64% | 100% |
A4H6N3 | Leishmania braziliensis | 43% | 100% |
A4HV16 | Leishmania infantum | 86% | 100% |
A4HV17 | Leishmania infantum | 45% | 100% |
E9ANQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4QGX2 | Leishmania major | 82% | 100% |