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: E9B3N8
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 | 108 | 112 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.804 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.825 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.818 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.642 |
CLV_PCSK_FUR_1 | 30 | 34 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.825 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.817 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.817 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.376 |
CLV_PCSK_PC7_1 | 33 | 39 | PF00082 | 0.590 |
CLV_Separin_Metazoa | 139 | 143 | PF03568 | 0.820 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.674 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.741 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.622 |
DOC_USP7_MATH_2 | 47 | 53 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.650 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.516 |
LIG_CaM_IQ_9 | 347 | 363 | PF13499 | 0.430 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.731 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.610 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.697 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.693 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.171 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.627 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.627 |
LIG_Pex14_1 | 22 | 26 | PF04695 | 0.622 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.376 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.514 |
LIG_SH3_1 | 193 | 199 | PF00018 | 0.610 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.773 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.682 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.629 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.716 |
LIG_SUMO_SIM_par_1 | 180 | 188 | PF11976 | 0.497 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.501 |
LIG_TRAF2_1 | 47 | 50 | PF00917 | 0.690 |
LIG_WW_3 | 139 | 143 | PF00397 | 0.820 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.639 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.765 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.568 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.430 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.723 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.730 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.665 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.801 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.616 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.171 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.762 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.589 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.818 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.678 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.713 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.706 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.607 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.793 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.376 |
MOD_GlcNHglycan | 49 | 54 | PF01048 | 0.730 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.517 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.621 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.756 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.613 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.479 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.430 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.454 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.708 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.604 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.557 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.376 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.430 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.557 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.786 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.577 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.376 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.742 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.753 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.523 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.732 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.612 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.523 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.810 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.689 |
TRG_DiLeu_BaEn_2 | 238 | 244 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_2 | 368 | 374 | PF01217 | 0.424 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.818 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.601 |
TRG_ER_diLys_1 | 377 | 380 | PF00400 | 0.596 |
TRG_NLS_Bipartite_1 | 192 | 211 | PF00514 | 0.813 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 340 | 344 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 7 | 11 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC1 | Leptomonas seymouri | 51% | 91% |
A0A3S7X6H7 | Leishmania donovani | 88% | 100% |
A0A422N868 | Trypanosoma rangeli | 33% | 100% |
A4HL96 | Leishmania braziliensis | 77% | 99% |
A4I8S2 | Leishmania infantum | 88% | 100% |
Q4Q4E9 | Leishmania major | 89% | 100% |