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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ATT1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.563 |
CLV_PCSK_FUR_1 | 115 | 119 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 253 | 259 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.466 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.521 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.444 |
DOC_CYCLIN_RxL_1 | 18 | 26 | PF00134 | 0.335 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 290 | 300 | PF00069 | 0.614 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.521 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.731 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.559 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 281 | 289 | PF00928 | 0.607 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.564 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.604 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.680 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.440 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.405 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.511 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 288 | 292 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 137 | 144 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.374 |
LIG_MAD2 | 21 | 29 | PF02301 | 0.516 |
LIG_MLH1_MIPbox_1 | 165 | 169 | PF16413 | 0.466 |
LIG_NRBOX | 305 | 311 | PF00104 | 0.625 |
LIG_PCNA_yPIPBox_3 | 303 | 315 | PF02747 | 0.633 |
LIG_PDZ_Class_1 | 343 | 348 | PF00595 | 0.446 |
LIG_Pex14_1 | 282 | 286 | PF04695 | 0.662 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.392 |
LIG_PTB_Apo_2 | 66 | 73 | PF02174 | 0.379 |
LIG_PTB_Phospho_1 | 66 | 72 | PF10480 | 0.376 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.423 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.564 |
LIG_SH2_GRB2like | 338 | 341 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 72 | 76 | PF00017 | 0.498 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 294 | 297 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.389 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.500 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.568 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.636 |
LIG_TRAF2_1 | 151 | 154 | PF00917 | 0.523 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.462 |
LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.437 |
LIG_TYR_ITSM | 68 | 75 | PF00017 | 0.495 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.395 |
MOD_CDK_SPK_2 | 310 | 315 | PF00069 | 0.682 |
MOD_CDK_SPxK_1 | 272 | 278 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.635 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.501 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.527 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.692 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.700 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.581 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.398 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.641 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.640 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.474 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.375 |
MOD_Cter_Amidation | 113 | 116 | PF01082 | 0.500 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.674 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.624 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.707 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.469 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.556 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.564 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.598 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.587 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.498 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.559 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.655 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.621 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.665 |
MOD_LATS_1 | 165 | 171 | PF00433 | 0.445 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.560 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.495 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.561 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.475 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.791 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.423 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.420 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.650 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.601 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.652 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.376 |
MOD_Plk_2-3 | 148 | 154 | PF00069 | 0.629 |
MOD_Plk_2-3 | 296 | 302 | PF00069 | 0.594 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.376 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.398 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.686 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.739 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.590 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.684 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.729 |
MOD_SUMO_rev_2 | 148 | 158 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_4 | 301 | 307 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.426 |
TRG_PTS1 | 345 | 348 | PF00515 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P554 | Leptomonas seymouri | 67% | 93% |
A0A1X0P394 | Trypanosomatidae | 41% | 88% |
A0A3Q8IRL6 | Leishmania donovani | 91% | 100% |
A0A3R7NA51 | Trypanosoma rangeli | 51% | 98% |
A4HQ14 | Leishmania braziliensis | 83% | 100% |
A4ICE4 | Leishmania infantum | 91% | 100% |
D0A8V6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
Q4Q0R5 | Leishmania major | 91% | 99% |
V5BDN3 | Trypanosoma cruzi | 49% | 100% |