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: A0A3S5H559
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 289 | 293 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.611 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.691 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.646 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.731 |
DOC_CYCLIN_RxL_1 | 379 | 389 | PF00134 | 0.686 |
DOC_CYCLIN_yCln2_LP_2 | 330 | 336 | PF00134 | 0.690 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.689 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.846 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.706 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 300 | 308 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 382 | 391 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 72 | 77 | PF00244 | 0.714 |
LIG_BIR_III_4 | 318 | 322 | PF00653 | 0.817 |
LIG_CSL_BTD_1 | 252 | 255 | PF09270 | 0.587 |
LIG_EH1_1 | 215 | 223 | PF00400 | 0.455 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.548 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.807 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.609 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.581 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.771 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.576 |
LIG_LIR_Gen_1 | 164 | 171 | PF02991 | 0.751 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.529 |
LIG_LIR_LC3C_4 | 116 | 121 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 14 | 19 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.520 |
LIG_NRBOX | 118 | 124 | PF00104 | 0.691 |
LIG_PCNA_yPIPBox_3 | 12 | 26 | PF02747 | 0.594 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.578 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.760 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 371 | 374 | PF00017 | 0.750 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.591 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.613 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.776 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.525 |
LIG_SUMO_SIM_par_1 | 118 | 125 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 332 | 337 | PF11976 | 0.691 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.451 |
LIG_TRFH_1 | 34 | 38 | PF08558 | 0.683 |
MOD_CDK_SPK_2 | 153 | 158 | PF00069 | 0.716 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.556 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.532 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.589 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.796 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.646 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.404 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.616 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.706 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.791 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.661 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.642 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.651 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.611 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.640 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.750 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.633 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.774 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.769 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.628 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.625 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.625 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.669 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.554 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.598 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.686 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.697 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.718 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.619 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.812 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.821 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.718 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.640 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.679 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.718 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.795 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.825 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.707 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.625 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.715 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.652 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.619 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.777 |
MOD_PK_1 | 72 | 78 | PF00069 | 0.717 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.828 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.590 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.623 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.746 |
MOD_Plk_2-3 | 314 | 320 | PF00069 | 0.642 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.596 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.660 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.642 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.638 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.562 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.752 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.623 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.705 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.710 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.737 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.741 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.651 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.677 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.616 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.824 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_1 | 389 | 394 | PF01217 | 0.623 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.707 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.520 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.759 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 382 | 387 | PF00026 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3J3 | Leptomonas seymouri | 47% | 95% |
A4H3P0 | Leishmania braziliensis | 72% | 97% |
A4HRW7 | Leishmania infantum | 100% | 100% |
E9ACM4 | Leishmania major | 94% | 100% |
E9AJW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |