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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HL96
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 8 |
GO:0005488 | binding | 1 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.817 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.846 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.819 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.655 |
CLV_PCSK_FUR_1 | 30 | 34 | PF00082 | 0.689 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.846 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.818 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.376 |
CLV_PCSK_PC7_1 | 32 | 38 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.439 |
CLV_Separin_Metazoa | 139 | 143 | PF03568 | 0.833 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.685 |
DEG_SCF_FBW7_1 | 57 | 62 | PF00400 | 0.481 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.746 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.642 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 89 | 98 | PF00244 | 0.548 |
LIG_CaM_IQ_9 | 345 | 361 | PF13499 | 0.430 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.708 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.738 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.472 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.672 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.751 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.684 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.171 |
LIG_Integrin_isoDGR_2 | 373 | 375 | PF01839 | 0.380 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.634 |
LIG_MYND_1 | 104 | 108 | PF01753 | 0.562 |
LIG_Pex14_1 | 22 | 26 | PF04695 | 0.626 |
LIG_Pex14_2 | 291 | 295 | PF04695 | 0.376 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.516 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.774 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.501 |
LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.706 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.619 |
LIG_WW_3 | 139 | 143 | PF00397 | 0.833 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.759 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.640 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.666 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.566 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.430 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.731 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.747 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.654 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.650 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.615 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.171 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.773 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.633 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.578 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.601 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.822 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.507 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.658 |
MOD_GlcNHglycan | 135 | 139 | PF01048 | 0.667 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.617 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.751 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.785 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.529 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.376 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.522 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.638 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.618 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.430 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.704 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.693 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.515 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.674 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.591 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.593 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.561 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.587 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.568 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.559 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.376 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.568 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.749 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.565 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.573 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.376 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.731 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.682 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.585 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.819 |
MOD_PKB_1 | 39 | 47 | PF00069 | 0.661 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.429 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.565 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.738 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.642 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.802 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.574 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.707 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.581 |
TRG_DiLeu_BaEn_1 | 367 | 372 | PF01217 | 0.249 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.819 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.614 |
TRG_NLS_Bipartite_1 | 192 | 211 | PF00514 | 0.831 |
TRG_Pf-PMV_PEXEL_1 | 338 | 342 | PF00026 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC1 | Leptomonas seymouri | 49% | 90% |
A0A3S7X6H7 | Leishmania donovani | 76% | 100% |
A0A422N868 | Trypanosoma rangeli | 34% | 100% |
A4I8S2 | Leishmania infantum | 76% | 100% |
E9B3N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 99% |
Q4Q4E9 | Leishmania major | 76% | 100% |