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 |
Related structures:
AlphaFold database: E9ASC4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.541 |
CLV_Separin_Metazoa | 190 | 194 | PF03568 | 0.336 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.588 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.640 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.620 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 36 | 42 | PF00134 | 0.656 |
DOC_MAPK_gen_1 | 29 | 38 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.636 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.603 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.649 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.536 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.661 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.376 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.550 |
LIG_14-3-3_CanoR_1 | 105 | 109 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 234 | 244 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 260 | 267 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.678 |
LIG_14-3-3_CterR_2 | 317 | 322 | PF00244 | 0.562 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.580 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.574 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.754 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.706 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.612 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.651 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.316 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.635 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.651 |
LIG_LIR_Apic_2 | 153 | 159 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.552 |
LIG_MYND_1 | 255 | 259 | PF01753 | 0.623 |
LIG_NRBOX | 187 | 193 | PF00104 | 0.336 |
LIG_PDZ_Class_2 | 317 | 322 | PF00595 | 0.610 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.530 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 156 | 160 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.515 |
LIG_SH3_1 | 156 | 162 | PF00018 | 0.481 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.602 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.510 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.665 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.656 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.656 |
LIG_SH3_CIN85_PxpxPR_1 | 158 | 163 | PF14604 | 0.593 |
LIG_WW_3 | 55 | 59 | PF00397 | 0.646 |
MOD_CDK_SPK_2 | 255 | 260 | PF00069 | 0.558 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.566 |
MOD_CDK_SPxxK_3 | 154 | 161 | PF00069 | 0.662 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.566 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.670 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.566 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.582 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.564 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.590 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.309 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.575 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.635 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.631 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.681 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.578 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.679 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.650 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.597 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.564 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.316 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.576 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.637 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.622 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.668 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.659 |
MOD_GlcNHglycan | 87 | 91 | PF01048 | 0.476 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.648 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.574 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.523 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.645 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.640 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.651 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.529 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.653 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.636 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.548 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.731 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.367 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.636 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.309 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.496 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.650 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.668 |
MOD_PK_1 | 195 | 201 | PF00069 | 0.328 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.527 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.362 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.641 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.709 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.587 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.584 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.608 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.561 |
MOD_PKB_1 | 193 | 201 | PF00069 | 0.328 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.489 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.563 |
MOD_Plk_2-3 | 144 | 150 | PF00069 | 0.677 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.637 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.563 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.661 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.519 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.566 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.499 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.661 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.643 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.623 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.622 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.546 |
MOD_SUMO_rev_2 | 181 | 191 | PF00179 | 0.273 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.517 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.295 |
TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.657 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.601 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.518 |
TRG_NLS_MonoExtN_4 | 3 | 9 | PF00514 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II75 | Leptomonas seymouri | 55% | 100% |
A0A1X0P8R1 | Trypanosomatidae | 30% | 100% |
A0A3S7XA97 | Leishmania donovani | 86% | 100% |
A4HNL1 | Leishmania braziliensis | 68% | 100% |
A4ICY1 | Leishmania infantum | 87% | 100% |
Q4Q272 | Leishmania major | 86% | 100% |