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:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3P0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.457 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.664 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.560 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.580 |
DEG_SPOP_SBC_1 | 306 | 310 | PF00917 | 0.585 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.492 |
DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.439 |
DOC_CYCLIN_RxL_1 | 392 | 402 | PF00134 | 0.579 |
DOC_PP1_RVXF_1 | 136 | 143 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.566 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.397 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 293 | 297 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 393 | 398 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 46 | 50 | PF00244 | 0.535 |
LIG_BIR_III_4 | 331 | 335 | PF00653 | 0.710 |
LIG_CSL_BTD_1 | 245 | 248 | PF09270 | 0.481 |
LIG_EVH1_1 | 253 | 257 | PF00568 | 0.527 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.570 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.816 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.527 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.572 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.540 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.528 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.632 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.675 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.449 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 191 | 202 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 216 | 224 | PF02991 | 0.452 |
LIG_LIR_LC3C_4 | 103 | 108 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.422 |
LIG_NRBOX | 105 | 111 | PF00104 | 0.550 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.592 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.432 |
LIG_SH2_NCK_1 | 154 | 158 | PF00017 | 0.424 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.463 |
LIG_SH3_1 | 253 | 259 | PF00018 | 0.595 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.762 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.421 |
LIG_SUMO_SIM_par_1 | 105 | 112 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 345 | 350 | PF11976 | 0.616 |
LIG_TRFH_1 | 34 | 38 | PF08558 | 0.620 |
MOD_CDK_SPK_2 | 140 | 145 | PF00069 | 0.585 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.466 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.521 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.521 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.672 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.569 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.726 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.387 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.755 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.546 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.542 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.452 |
MOD_DYRK1A_RPxSP_1 | 342 | 346 | PF00069 | 0.549 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.517 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.455 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.711 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.563 |
MOD_GlcNHglycan | 281 | 287 | PF01048 | 0.574 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.555 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.785 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.626 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.590 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.621 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.583 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.623 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.725 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.558 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.531 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.777 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.752 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.633 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.598 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.446 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.720 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.584 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.606 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.461 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.500 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.687 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.589 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.546 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.702 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.714 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.586 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.534 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.445 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.521 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.445 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.531 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.499 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.661 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.583 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.620 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.668 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.569 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.757 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.689 |
MOD_SUMO_rev_2 | 323 | 330 | PF00179 | 0.569 |
TRG_AP2beta_CARGO_1 | 14 | 23 | PF09066 | 0.391 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_1 | 402 | 407 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 395 | 400 | PF00026 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 419 | 423 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3J3 | Leptomonas seymouri | 45% | 98% |
A0A3S5H559 | Leishmania donovani | 72% | 100% |
A4HRW7 | Leishmania infantum | 71% | 100% |
E9ACM4 | Leishmania major | 73% | 94% |
E9AJW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |