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: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: A4HH87
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 649 | 651 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 238 | 246 | PF00400 | 0.598 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.575 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.635 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.676 |
DEG_SPOP_SBC_1 | 485 | 489 | PF00917 | 0.511 |
DOC_CDC14_PxL_1 | 451 | 459 | PF14671 | 0.675 |
DOC_CYCLIN_RxL_1 | 409 | 418 | PF00134 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 353 | 356 | PF00134 | 0.634 |
DOC_MAPK_gen_1 | 202 | 208 | PF00069 | 0.563 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.503 |
DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.676 |
DOC_PP4_FxxP_1 | 521 | 524 | PF00568 | 0.598 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.504 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.699 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 437 | 443 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 346 | 363 | PF00022 | 0.673 |
LIG_Actin_WH2_2 | 382 | 399 | PF00022 | 0.557 |
LIG_APCC_ABBAyCdc20_2 | 191 | 197 | PF00400 | 0.539 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.660 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.616 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.580 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.606 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.649 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.507 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.650 |
LIG_GBD_Chelix_1 | 331 | 339 | PF00786 | 0.558 |
LIG_Integrin_isoDGR_2 | 373 | 375 | PF01839 | 0.512 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.670 |
LIG_LIR_Apic_2 | 518 | 524 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 164 | 174 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 326 | 335 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.647 |
LIG_MLH1_MIPbox_1 | 448 | 452 | PF16413 | 0.660 |
LIG_MYND_1 | 604 | 608 | PF01753 | 0.529 |
LIG_NRP_CendR_1 | 649 | 652 | PF00754 | 0.719 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.459 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.608 |
LIG_SH2_GRB2like | 207 | 210 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.632 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.699 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.480 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.673 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.769 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.641 |
LIG_UBA3_1 | 241 | 249 | PF00899 | 0.587 |
LIG_WRC_WIRS_1 | 190 | 195 | PF05994 | 0.574 |
LIG_WW_2 | 455 | 458 | PF00397 | 0.668 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.609 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.587 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.591 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.575 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.630 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.583 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.549 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.429 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.572 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.669 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.602 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.516 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.798 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.557 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.644 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.619 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.545 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.663 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.541 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.755 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.506 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.702 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.703 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.644 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.564 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.727 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.616 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.417 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.678 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.533 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.766 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.507 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.563 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.576 |
MOD_N-GLC_2 | 310 | 312 | PF02516 | 0.511 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.667 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.735 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.772 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.656 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.639 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.587 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.497 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.500 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.579 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.573 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.528 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.491 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.714 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.561 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.453 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.607 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.609 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.662 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.529 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.668 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.528 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.482 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.693 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.649 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.607 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.648 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.555 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.529 |
TRG_DiLeu_BaEn_2 | 188 | 194 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.568 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.798 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 649 | 652 | PF00400 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 239 | 244 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3R7L5N2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X2B5 | Leishmania donovani | 81% | 99% |
A4I4D3 | Leishmania infantum | 78% | 93% |
E9ADT2 | Leishmania major | 82% | 100% |
E9ALZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 97% |