Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.800 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.795 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.573 |
CLV_PCSK_FUR_1 | 297 | 301 | PF00082 | 0.792 |
CLV_PCSK_FUR_1 | 321 | 325 | PF00082 | 0.796 |
CLV_PCSK_FUR_1 | 334 | 338 | PF00082 | 0.641 |
CLV_PCSK_FUR_1 | 361 | 365 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.800 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.770 |
CLV_PCSK_PC7_1 | 265 | 271 | PF00082 | 0.780 |
CLV_PCSK_PC7_1 | 289 | 295 | PF00082 | 0.762 |
CLV_PCSK_PC7_1 | 356 | 362 | PF00082 | 0.785 |
CLV_PCSK_PC7_1 | 364 | 370 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.609 |
DEG_APCC_KENBOX_2 | 155 | 159 | PF00400 | 0.680 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.552 |
DOC_MAPK_gen_1 | 138 | 145 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.604 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.761 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.829 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.793 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.841 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.833 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.609 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.770 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.565 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.597 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.598 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.507 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.533 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.671 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.545 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.783 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.593 |
LIG_GBD_Chelix_1 | 232 | 240 | PF00786 | 0.602 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.723 |
LIG_NRP_CendR_1 | 369 | 372 | PF00754 | 0.760 |
LIG_PTB_Apo_2 | 131 | 138 | PF02174 | 0.585 |
LIG_PTB_Phospho_1 | 131 | 137 | PF10480 | 0.568 |
LIG_SH2_GRB2like | 176 | 179 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.443 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.783 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.655 |
LIG_SH3_2 | 65 | 70 | PF14604 | 0.743 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.758 |
MOD_CDC14_SPxK_1 | 260 | 263 | PF00782 | 0.774 |
MOD_CDK_SPxK_1 | 257 | 263 | PF00069 | 0.769 |
MOD_CDK_SPxxK_3 | 300 | 307 | PF00069 | 0.787 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.659 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.872 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.820 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.838 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.683 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.619 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.598 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.624 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.654 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.581 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.738 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.611 |
MOD_Cter_Amidation | 321 | 324 | PF01082 | 0.797 |
MOD_DYRK1A_RPxSP_1 | 300 | 304 | PF00069 | 0.785 |
MOD_DYRK1A_RPxSP_1 | 324 | 328 | PF00069 | 0.794 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.668 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.626 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.655 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.749 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.772 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.815 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.740 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.650 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.635 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.787 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.793 |
MOD_LATS_1 | 281 | 287 | PF00433 | 0.791 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.481 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.443 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.799 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.553 |
MOD_NEK2_2 | 195 | 200 | PF00069 | 0.481 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.725 |
MOD_PKA_1 | 283 | 289 | PF00069 | 0.793 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.788 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.854 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.727 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.644 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.834 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.795 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.643 |
MOD_PKB_1 | 283 | 291 | PF00069 | 0.792 |
MOD_PKB_1 | 315 | 323 | PF00069 | 0.793 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.609 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.490 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.418 |
MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.566 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.605 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.618 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.831 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.785 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.807 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.794 |
MOD_SUMO_rev_2 | 222 | 232 | PF00179 | 0.451 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.681 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.797 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.755 |
TRG_NLS_MonoCore_2 | 158 | 163 | PF00514 | 0.694 |
TRG_NLS_MonoExtC_3 | 158 | 164 | PF00514 | 0.694 |
TRG_NLS_MonoExtN_4 | 156 | 163 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 126 | 131 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 245 | 249 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPZ1 | Leishmania donovani | 93% | 99% |
A4H537 | Leishmania braziliensis | 79% | 100% |
A4HTB3 | Leishmania infantum | 93% | 99% |
Q4QIK0 | Leishmania major | 93% | 100% |