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 | yes | yes: 3, no: 6 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ATT4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.526 |
CLV_PCSK_FUR_1 | 344 | 348 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.427 |
CLV_PCSK_PC7_1 | 341 | 347 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.432 |
DEG_MDM2_SWIB_1 | 135 | 142 | PF02201 | 0.539 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.515 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 27 | PF00134 | 0.519 |
DOC_MAPK_FxFP_2 | 218 | 221 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 113 | 121 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 254 | 263 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 341 | 351 | PF00069 | 0.744 |
DOC_MAPK_gen_1 | 4 | 10 | PF00069 | 0.403 |
DOC_MAPK_JIP1_4 | 247 | 253 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 116 | 122 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 201 | 207 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.510 |
DOC_PP4_FxxP_1 | 218 | 221 | PF00568 | 0.479 |
DOC_SPAK_OSR1_1 | 239 | 243 | PF12202 | 0.457 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.592 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 226 | 230 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 280 | 286 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 79 | 83 | PF00244 | 0.438 |
LIG_APCC_ABBA_1 | 212 | 217 | PF00400 | 0.499 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.740 |
LIG_BIR_III_4 | 88 | 92 | PF00653 | 0.585 |
LIG_EH_1 | 73 | 77 | PF12763 | 0.688 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.570 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.517 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.580 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.585 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.548 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 40 | 48 | PF02991 | 0.567 |
LIG_LIR_LC3C_4 | 260 | 263 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.558 |
LIG_PCNA_PIPBox_1 | 234 | 243 | PF02747 | 0.564 |
LIG_PCNA_yPIPBox_3 | 231 | 241 | PF02747 | 0.549 |
LIG_PDZ_Class_2 | 347 | 352 | PF00595 | 0.662 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.539 |
LIG_SH2_SRC | 184 | 187 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.493 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.714 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 16 | 22 | PF11976 | 0.573 |
LIG_SUMO_SIM_anti_2 | 210 | 215 | PF11976 | 0.508 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.634 |
LIG_SUMO_SIM_par_1 | 23 | 28 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 259 | 265 | PF11976 | 0.639 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.565 |
LIG_ULM_U2AF65_1 | 344 | 349 | PF00076 | 0.766 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.608 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.530 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.755 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.495 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.484 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.519 |
MOD_Cter_Amidation | 167 | 170 | PF01082 | 0.636 |
MOD_Cter_Amidation | 342 | 345 | PF01082 | 0.642 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.640 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.622 |
MOD_GlcNHglycan | 317 | 321 | PF01048 | 0.681 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.648 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.630 |
MOD_GlcNHglycan | 34 | 38 | PF01048 | 0.479 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.571 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.704 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.576 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.697 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.688 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.656 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.622 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.404 |
MOD_N-GLC_2 | 56 | 58 | PF02516 | 0.421 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.526 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.508 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.475 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.586 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.606 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.403 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.447 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.403 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.546 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.554 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.645 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.674 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.421 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.646 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.609 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.301 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.540 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.531 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.471 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.519 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.530 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.531 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.546 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.519 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.683 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 246 | 251 | PF01217 | 0.596 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 253 | 256 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.690 |
TRG_NES_CRM1_1 | 265 | 276 | PF08389 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVC1 | Leptomonas seymouri | 53% | 100% |
A0A1X0P309 | Trypanosomatidae | 29% | 100% |
A0A3Q8IJW1 | Leishmania donovani | 91% | 100% |
A0A3R7KTI3 | Trypanosoma rangeli | 26% | 100% |
A4HQ17 | Leishmania braziliensis | 73% | 100% |
A4IDS3 | Leishmania infantum | 91% | 100% |
Q4Q0R2 | Leishmania major | 86% | 100% |
V5D4Y6 | Trypanosoma cruzi | 25% | 100% |