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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001917 | photoreceptor inner segment | 2 | 10 |
GO:0005737 | cytoplasm | 2 | 10 |
GO:0005829 | cytosol | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q2P1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.755 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.598 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.712 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.699 |
DOC_CKS1_1 | 156 | 161 | PF01111 | 0.618 |
DOC_MAPK_DCC_7 | 127 | 135 | PF00069 | 0.734 |
DOC_MAPK_gen_1 | 338 | 344 | PF00069 | 0.604 |
DOC_MAPK_HePTP_8 | 224 | 236 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 227 | 236 | PF00069 | 0.556 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.701 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.688 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 261 | 270 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 282 | 290 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 82 | 86 | PF00244 | 0.606 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.561 |
LIG_BIR_III_4 | 94 | 98 | PF00653 | 0.784 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.576 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.666 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.536 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.492 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.490 |
LIG_Pex14_2 | 131 | 135 | PF04695 | 0.686 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 145 | 149 | PF00017 | 0.721 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.499 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.613 |
LIG_UBA3_1 | 7 | 15 | PF00899 | 0.580 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.593 |
MOD_CDK_SPxxK_3 | 155 | 162 | PF00069 | 0.628 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.704 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.733 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.575 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.508 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.485 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.709 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.655 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.665 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.699 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.694 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.727 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.642 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.586 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.716 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.224 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.391 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.287 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.267 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.713 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.745 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.690 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.364 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.424 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.724 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.483 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.727 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.676 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.661 |
MOD_N-GLC_2 | 18 | 20 | PF02516 | 0.681 |
MOD_N-GLC_2 | 206 | 208 | PF02516 | 0.331 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.743 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.536 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.490 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.548 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.570 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.676 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.771 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.474 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.591 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.698 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.707 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.721 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.562 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.591 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.765 |
MOD_Plk_2-3 | 179 | 185 | PF00069 | 0.481 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.688 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.529 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.646 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.621 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.531 |
TRG_DiLeu_BaEn_1 | 3 | 8 | PF01217 | 0.687 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.777 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P513 | Leptomonas seymouri | 52% | 95% |
A0A1X0P9U1 | Trypanosomatidae | 38% | 100% |
A0A3S7X892 | Leishmania donovani | 92% | 100% |
A0A422N4K3 | Trypanosoma rangeli | 41% | 100% |
A4HB22 | Leishmania braziliensis | 71% | 100% |
A4IA79 | Leishmania infantum | 91% | 100% |
C9ZM30 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B592 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |