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:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AYR9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.683 |
CLV_PCSK_FUR_1 | 15 | 19 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.381 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.546 |
DEG_SPOP_SBC_1 | 212 | 216 | PF00917 | 0.411 |
DEG_SPOP_SBC_1 | 223 | 227 | PF00917 | 0.252 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.445 |
DOC_CYCLIN_RxL_1 | 382 | 392 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 358 | 368 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.505 |
DOC_MAPK_RevD_3 | 149 | 164 | PF00069 | 0.432 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.631 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.375 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 112 | 121 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 347 | 357 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 415 | 419 | PF00244 | 0.698 |
LIG_BRCT_BRCA1_1 | 187 | 191 | PF00533 | 0.370 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 441 | 445 | PF00533 | 0.457 |
LIG_Clathr_ClatBox_1 | 406 | 410 | PF01394 | 0.342 |
LIG_Clathr_ClatBox_1 | 87 | 91 | PF01394 | 0.450 |
LIG_CtBP_PxDLS_1 | 153 | 157 | PF00389 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 240 | 250 | PF00928 | 0.276 |
LIG_eIF4E_1 | 433 | 439 | PF01652 | 0.715 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.434 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.347 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.438 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.559 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.308 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.421 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.389 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.192 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.421 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.544 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.416 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.456 |
LIG_LIR_Gen_1 | 240 | 251 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.485 |
LIG_SH2_GRB2like | 237 | 240 | PF00017 | 0.266 |
LIG_SH2_PTP2 | 343 | 346 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.344 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.489 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.410 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.632 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.449 |
LIG_SUMO_SIM_anti_2 | 396 | 403 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 119 | 125 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 225 | 235 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 396 | 403 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.498 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.431 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.294 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.471 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.396 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.361 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.351 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.388 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.425 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.328 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.367 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.382 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.457 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.435 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.728 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.637 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.560 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.657 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.451 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.575 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.577 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.693 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.335 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.418 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.398 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.385 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.404 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.420 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.464 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.355 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.429 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.397 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.423 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.630 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.392 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.413 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.589 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.531 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.514 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.419 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.403 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.295 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.352 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.412 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.390 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.227 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.572 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.433 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.336 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.478 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.375 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.544 |
MOD_PKA_1 | 163 | 169 | PF00069 | 0.470 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.345 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.478 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.678 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.504 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.516 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.434 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.520 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.469 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.407 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.412 |
MOD_Plk_2-3 | 8 | 14 | PF00069 | 0.476 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.330 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.354 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.347 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.355 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.470 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.398 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.207 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 155 | 165 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 402 | 407 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.481 |
TRG_NLS_MonoExtC_3 | 357 | 363 | PF00514 | 0.545 |
TRG_NLS_MonoExtN_4 | 357 | 362 | PF00514 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAF2 | Leptomonas seymouri | 63% | 99% |
A0A1X0NLR9 | Trypanosomatidae | 27% | 86% |
A0A3Q8ID84 | Leishmania donovani | 94% | 100% |
A0A422NXM8 | Trypanosoma rangeli | 30% | 86% |
A4HFD5 | Leishmania braziliensis | 83% | 100% |
A4I359 | Leishmania infantum | 94% | 100% |
C9ZKV6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 85% |
E9ACZ4 | Leishmania major | 94% | 100% |
V5BKT2 | Trypanosoma cruzi | 27% | 86% |