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: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A0A3Q8ID09
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.312 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.330 |
CLV_PCSK_PC7_1 | 153 | 159 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 122 | 130 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.438 |
DOC_AGCK_PIF_1 | 213 | 218 | PF00069 | 0.426 |
DOC_MAPK_DCC_7 | 224 | 233 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 257 | 265 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 286 | 293 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 66 | 73 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.435 |
DOC_MAPK_RevD_3 | 53 | 67 | PF00069 | 0.322 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.269 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.340 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 131 | 139 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 185 | 193 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 236 | 245 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 81 | 89 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.406 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.322 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.460 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.485 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.320 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.344 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.433 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.490 |
LIG_Integrin_isoDGR_2 | 100 | 102 | PF01839 | 0.350 |
LIG_LIR_Apic_2 | 359 | 363 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 272 | 279 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.647 |
LIG_PCNA_yPIPBox_3 | 149 | 163 | PF02747 | 0.286 |
LIG_Pex14_2 | 105 | 109 | PF04695 | 0.316 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.427 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.320 |
LIG_PTB_Apo_2 | 138 | 145 | PF02174 | 0.406 |
LIG_PTB_Phospho_1 | 138 | 144 | PF10480 | 0.406 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.406 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.286 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 360 | 363 | PF00017 | 0.655 |
LIG_SH2_SRC | 40 | 43 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.176 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.280 |
LIG_SH3_1 | 360 | 366 | PF00018 | 0.610 |
LIG_SH3_2 | 4 | 9 | PF14604 | 0.596 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.649 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.524 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.444 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.582 |
LIG_TYR_ITIM | 243 | 248 | PF00017 | 0.406 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.409 |
LIG_WW_3 | 182 | 186 | PF00397 | 0.322 |
MOD_CDK_SPxxK_3 | 18 | 25 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.616 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.532 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.319 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.337 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.368 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.395 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.372 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.271 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.325 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.286 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.358 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.398 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.492 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.365 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.518 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.589 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.378 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.454 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.344 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.370 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.385 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.582 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.271 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.431 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.259 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.441 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.484 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.457 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.306 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.372 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.389 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.321 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.453 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.487 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.441 |
TRG_NLS_MonoExtC_3 | 256 | 262 | PF00514 | 0.286 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAU5 | Leptomonas seymouri | 83% | 100% |
A0A0S4IIH8 | Bodo saltans | 27% | 100% |
A0A0S4JB96 | Bodo saltans | 47% | 100% |
A0A0S4JFE6 | Bodo saltans | 28% | 94% |
A0A1X0NIK1 | Trypanosomatidae | 25% | 68% |
A0A1X0NVZ5 | Trypanosomatidae | 56% | 96% |
A0A422NWK7 | Trypanosoma rangeli | 56% | 96% |
A4HDS0 | Leishmania braziliensis | 97% | 100% |
A4I118 | Leishmania infantum | 100% | 100% |
C9ZHV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 89% |
C9ZW92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 96% |
E9AX55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
O04318 | Arabidopsis thaliana | 21% | 81% |
O49326 | Arabidopsis thaliana | 23% | 80% |
Q0IIC2 | Bos taurus | 25% | 86% |
Q10AZ7 | Oryza sativa subsp. japonica | 27% | 75% |
Q28DE7 | Xenopus tropicalis | 25% | 92% |
Q3KRE6 | Rattus norvegicus | 25% | 93% |
Q4G5Y1 | Mus musculus | 25% | 93% |
Q4QAC1 | Leishmania major | 100% | 100% |
Q4V8F4 | Rattus norvegicus | 26% | 100% |
Q58CV6 | Bos taurus | 27% | 99% |
Q5E9A7 | Bos taurus | 25% | 93% |
Q5EA50 | Bos taurus | 25% | 100% |
Q5U3Y0 | Rattus norvegicus | 24% | 92% |
Q5U580 | Xenopus laevis | 25% | 92% |
Q5ZJ37 | Gallus gallus | 24% | 100% |
Q6AXB2 | Xenopus laevis | 24% | 100% |
Q6PAR0 | Mus musculus | 25% | 86% |
Q6PID8 | Homo sapiens | 25% | 86% |
Q7Z6M1 | Homo sapiens | 26% | 100% |
Q80YG3 | Mus musculus | 25% | 93% |
Q8N7A1 | Homo sapiens | 25% | 93% |
Q8TBB5 | Homo sapiens | 24% | 73% |
Q8VCH5 | Mus musculus | 25% | 99% |
Q9BQ90 | Homo sapiens | 27% | 99% |
Q9SDM9 | Arabidopsis thaliana | 21% | 80% |
Q9Y2U9 | Homo sapiens | 25% | 93% |
V5BAH1 | Trypanosoma cruzi | 55% | 96% |
V5BAQ7 | Trypanosoma cruzi | 25% | 78% |
V5DS74 | Trypanosoma cruzi | 24% | 94% |