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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0044613 | nuclear pore central transport channel | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9ALZ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 247 | 255 | PF00400 | 0.612 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.706 |
DOC_CDC14_PxL_1 | 460 | 468 | PF14671 | 0.707 |
DOC_CYCLIN_yCln2_LP_2 | 362 | 365 | PF00134 | 0.657 |
DOC_MAPK_gen_1 | 211 | 217 | PF00069 | 0.583 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.617 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.657 |
DOC_PP4_FxxP_1 | 461 | 464 | PF00568 | 0.703 |
DOC_PP4_FxxP_1 | 530 | 533 | PF00568 | 0.688 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.690 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.578 |
LIG_Actin_WH2_2 | 306 | 323 | PF00022 | 0.485 |
LIG_Actin_WH2_2 | 355 | 372 | PF00022 | 0.657 |
LIG_Actin_WH2_2 | 391 | 408 | PF00022 | 0.492 |
LIG_APCC_ABBAyCdc20_2 | 200 | 206 | PF00400 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.687 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.684 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.595 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.639 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.518 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.609 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.693 |
LIG_GBD_Chelix_1 | 340 | 348 | PF00786 | 0.585 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.697 |
LIG_LIR_Apic_2 | 527 | 533 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.733 |
LIG_LIR_Gen_1 | 335 | 344 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.696 |
LIG_LYPXL_yS_3 | 158 | 161 | PF13949 | 0.594 |
LIG_MLH1_MIPbox_1 | 457 | 461 | PF16413 | 0.687 |
LIG_NRP_CendR_1 | 671 | 673 | PF00754 | 0.749 |
LIG_PTAP_UEV_1 | 621 | 626 | PF05743 | 0.652 |
LIG_REV1ctd_RIR_1 | 423 | 432 | PF16727 | 0.462 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.618 |
LIG_SH2_GRB2like | 216 | 219 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.703 |
LIG_SH3_2 | 365 | 370 | PF14604 | 0.567 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.758 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.579 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.559 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.706 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.503 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.702 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.628 |
LIG_UBA3_1 | 250 | 258 | PF00899 | 0.607 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.577 |
LIG_WW_2 | 464 | 467 | PF00397 | 0.709 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.763 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.618 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.593 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.600 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.690 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.629 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.558 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.600 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.632 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.602 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.600 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.652 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.692 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.588 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.667 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.526 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.656 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.735 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.669 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.613 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.613 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.657 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.556 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.730 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.760 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.633 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.671 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.583 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.663 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.667 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.568 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.628 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.607 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.645 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.517 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.618 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.542 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.675 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.379 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.676 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.635 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.564 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.618 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.570 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.603 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.694 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.508 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.742 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.722 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.554 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.385 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.638 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.430 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.572 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.558 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.759 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.690 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.544 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.790 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.625 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.674 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.577 |
TRG_DiLeu_BaEn_2 | 197 | 203 | PF01217 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.666 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.707 |
TRG_Pf-PMV_PEXEL_1 | 248 | 253 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X2B5 | Leishmania donovani | 78% | 100% |
A4HH87 | Leishmania braziliensis | 78% | 100% |
A4I4D3 | Leishmania infantum | 78% | 96% |
E9ADT2 | Leishmania major | 88% | 100% |