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: E9AV19
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.419 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.519 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.496 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.376 |
DOC_CKS1_1 | 340 | 345 | PF01111 | 0.425 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.275 |
DOC_MAPK_gen_1 | 33 | 43 | PF00069 | 0.398 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.329 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.435 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 157 | 167 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 218 | 222 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 285 | 292 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 318 | 328 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 252 | 267 | PF00022 | 0.467 |
LIG_BIR_III_4 | 359 | 363 | PF00653 | 0.474 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.552 |
LIG_EH1_1 | 232 | 240 | PF00400 | 0.485 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.421 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.384 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.448 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.432 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.541 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.514 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 222 | 228 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 429 | 435 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.468 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.403 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.374 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 87 | 90 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.452 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.443 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.523 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.390 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.379 |
LIG_Sin3_3 | 74 | 81 | PF02671 | 0.341 |
LIG_SUMO_SIM_anti_2 | 246 | 251 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 73 | 80 | PF11976 | 0.336 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.345 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.564 |
LIG_TRFH_1 | 7 | 11 | PF08558 | 0.449 |
LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.390 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.261 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.453 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.560 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.518 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.442 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.460 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.314 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.514 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.522 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.506 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.595 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.517 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.606 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.579 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.494 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.534 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.386 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.362 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.518 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.477 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.607 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.447 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.431 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.683 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.714 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.491 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.399 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.504 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.408 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.373 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.572 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.399 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.512 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.372 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.387 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.657 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.459 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.513 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.507 |
MOD_PKA_1 | 317 | 323 | PF00069 | 0.582 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.426 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.288 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.417 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.465 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.531 |
MOD_PKB_1 | 33 | 41 | PF00069 | 0.408 |
MOD_PKB_1 | 368 | 376 | PF00069 | 0.420 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.501 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.432 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.491 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.371 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.408 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.435 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.509 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.462 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.469 |
TRG_DiLeu_BaEn_4 | 236 | 242 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 15 | 20 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P853 | Leptomonas seymouri | 53% | 88% |
A0A1X0NY38 | Trypanosomatidae | 30% | 100% |
A0A3Q8IDW0 | Leishmania donovani | 94% | 100% |
A0A422NBK7 | Trypanosoma rangeli | 30% | 100% |
A4HBP9 | Leishmania braziliensis | 86% | 99% |
A4HZ51 | Leishmania infantum | 94% | 100% |
D0A1Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4QCG3 | Leishmania major | 95% | 100% |
V5BQ65 | Trypanosoma cruzi | 28% | 100% |