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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0031080 | nuclear pore outer ring | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HBP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.578 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.315 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.507 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.334 |
DOC_CKS1_1 | 334 | 339 | PF01111 | 0.426 |
DOC_MAPK_gen_1 | 3 | 10 | PF00069 | 0.284 |
DOC_MAPK_gen_1 | 402 | 409 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 432 | 438 | PF00149 | 0.222 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.548 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.329 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.332 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 151 | 161 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 312 | 322 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.317 |
LIG_Actin_WH2_2 | 246 | 261 | PF00022 | 0.468 |
LIG_BIR_III_2 | 99 | 103 | PF00653 | 0.358 |
LIG_BIR_III_4 | 353 | 357 | PF00653 | 0.470 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.461 |
LIG_EH1_1 | 226 | 234 | PF00400 | 0.487 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.432 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.406 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.445 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.433 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.545 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.521 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.537 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 423 | 429 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.477 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.411 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.436 |
LIG_SH2_GRB2like | 370 | 373 | PF00017 | 0.466 |
LIG_SH2_PTP2 | 87 | 90 | PF00017 | 0.462 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.566 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.462 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.508 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.294 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.527 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.396 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.366 |
LIG_SUMO_SIM_anti_2 | 240 | 245 | PF11976 | 0.468 |
LIG_SUMO_SIM_anti_2 | 73 | 80 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 405 | 411 | PF11976 | 0.372 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.345 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.567 |
LIG_TRFH_1 | 7 | 11 | PF08558 | 0.436 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.393 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.430 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.398 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.457 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.590 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.438 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.450 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.307 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.527 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.521 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.607 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.589 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.545 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.399 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.521 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.474 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.606 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.463 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.440 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.349 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.692 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.420 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.722 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.406 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.502 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.418 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.370 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.574 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.373 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.551 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.408 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.407 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.516 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.388 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.402 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.670 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.465 |
MOD_NEK2_2 | 278 | 283 | PF00069 | 0.287 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.510 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.522 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.566 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.315 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.459 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.514 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.448 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.502 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.382 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.397 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.313 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.340 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.498 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.544 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.463 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P853 | Leptomonas seymouri | 52% | 87% |
A0A1X0NY38 | Trypanosomatidae | 30% | 100% |
A0A3Q8IDW0 | Leishmania donovani | 87% | 99% |
A0A422NBK7 | Trypanosoma rangeli | 30% | 100% |
A4HZ51 | Leishmania infantum | 87% | 99% |
D0A1Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AV19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4QCG3 | Leishmania major | 85% | 100% |
V5BQ65 | Trypanosoma cruzi | 27% | 100% |