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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AU50
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.335 |
CLV_TASPASE1 | 58 | 64 | PF01112 | 0.687 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.730 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.718 |
DOC_CYCLIN_RxL_1 | 50 | 60 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.584 |
DOC_MAPK_FxFP_2 | 350 | 353 | PF00069 | 0.214 |
DOC_MAPK_gen_1 | 102 | 111 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 293 | 303 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.524 |
DOC_MAPK_RevD_3 | 322 | 336 | PF00069 | 0.520 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.730 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.768 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.518 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 101 | 107 | PF00928 | 0.666 |
LIG_deltaCOP1_diTrp_1 | 146 | 153 | PF00928 | 0.696 |
LIG_EH1_1 | 315 | 323 | PF00400 | 0.565 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.750 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.636 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.651 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.525 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.743 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.659 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 151 | 156 | PF02991 | 0.734 |
LIG_LIR_Apic_2 | 265 | 270 | PF02991 | 0.606 |
LIG_LIR_Apic_2 | 283 | 287 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 146 | 157 | PF02991 | 0.735 |
LIG_LIR_Gen_1 | 19 | 27 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.784 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.214 |
LIG_LYPXL_SIV_4 | 72 | 80 | PF13949 | 0.526 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.511 |
LIG_PDZ_Class_2 | 357 | 362 | PF00595 | 0.335 |
LIG_Pex14_1 | 149 | 153 | PF04695 | 0.739 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.214 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.521 |
LIG_SH2_GRB2like | 298 | 301 | PF00017 | 0.546 |
LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.603 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.603 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.548 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.728 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.655 |
LIG_SUMO_SIM_par_1 | 83 | 90 | PF11976 | 0.522 |
LIG_TYR_ITIM | 289 | 294 | PF00017 | 0.458 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.348 |
LIG_UBA3_1 | 94 | 100 | PF00899 | 0.518 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.677 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.694 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.717 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.613 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.744 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.402 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.382 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.690 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.469 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.594 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.448 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.577 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.735 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.613 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.620 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.627 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.684 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.574 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.623 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.720 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.626 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.494 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.594 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.659 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.611 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.613 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.603 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.602 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.654 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.680 |
MOD_N-GLC_2 | 212 | 214 | PF02516 | 0.497 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.496 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.613 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.655 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.608 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.674 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.427 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.380 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.548 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.756 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.615 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.568 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.677 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.773 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.682 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.551 |
MOD_Plk_2-3 | 16 | 22 | PF00069 | 0.462 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.439 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.566 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.509 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.636 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.397 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.375 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.324 |
TRG_DiLeu_BaEn_1 | 90 | 95 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_4 | 329 | 335 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.346 |
TRG_DiLeu_BaLyEn_6 | 350 | 355 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.487 |
TRG_NES_CRM1_1 | 46 | 60 | PF08389 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I247 | Leptomonas seymouri | 41% | 100% |
A0A3S7XC14 | Leishmania donovani | 85% | 100% |
A4HQD4 | Leishmania braziliensis | 63% | 99% |
A4IE26 | Leishmania infantum | 85% | 100% |
Q4Q0E5 | Leishmania major | 85% | 100% |