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 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031965 | nuclear membrane | 4 | 1 |
Related structures:
AlphaFold database: A4HMB5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.335 |
CLV_PCSK_FUR_1 | 41 | 45 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.524 |
CLV_Separin_Metazoa | 230 | 234 | PF03568 | 0.533 |
DEG_APCC_DBOX_1 | 386 | 394 | PF00400 | 0.290 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.527 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.643 |
DEG_SPOP_SBC_1 | 317 | 321 | PF00917 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 259 | 265 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 196 | 206 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 40 | 50 | PF00069 | 0.545 |
DOC_PP2B_LxvP_1 | 258 | 261 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.582 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 245 | 255 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.629 |
LIG_Clathr_ClatBox_1 | 373 | 377 | PF01394 | 0.513 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.466 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.494 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.408 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.494 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.481 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.411 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.791 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.583 |
LIG_GBD_Chelix_1 | 292 | 300 | PF00786 | 0.756 |
LIG_GBD_Chelix_1 | 368 | 376 | PF00786 | 0.402 |
LIG_LIR_Apic_2 | 212 | 218 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 339 | 347 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 339 | 343 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 370 | 374 | PF02991 | 0.513 |
LIG_Pex14_2 | 392 | 396 | PF04695 | 0.474 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.753 |
LIG_REV1ctd_RIR_1 | 9 | 18 | PF16727 | 0.476 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.762 |
LIG_SH2_PTP2 | 340 | 343 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 19 | 23 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 301 | 304 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.474 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.780 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.666 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.599 |
LIG_SUMO_SIM_anti_2 | 339 | 345 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 365 | 370 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 370 | 378 | PF11976 | 0.416 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.821 |
LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.688 |
LIG_TRFH_1 | 33 | 37 | PF08558 | 0.613 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.238 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.513 |
MOD_CDK_SPxK_1 | 126 | 132 | PF00069 | 0.640 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.823 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.588 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.261 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.467 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.492 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.465 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.751 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.790 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.606 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.523 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.624 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.530 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.508 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.508 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.488 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.411 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.563 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.756 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.707 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.612 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.769 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.571 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.724 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.541 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.467 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.597 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.701 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.261 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.556 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.554 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.521 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.564 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.433 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.689 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.628 |
MOD_OFUCOSY | 348 | 354 | PF10250 | 0.411 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.766 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.455 |
MOD_PK_1 | 243 | 249 | PF00069 | 0.438 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.755 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.513 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.536 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.569 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.546 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.727 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.488 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.640 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.478 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.597 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.468 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.405 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.513 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.375 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.703 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.751 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.787 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.625 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.494 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.712 |
TRG_DiLeu_BaEn_1 | 2 | 7 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.623 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.722 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHG2 | Leptomonas seymouri | 44% | 95% |
A0A3Q8IP51 | Leishmania donovani | 70% | 96% |
A4IAY1 | Leishmania infantum | 70% | 96% |
E9AEQ9 | Leishmania major | 67% | 100% |
E9B5W4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 96% |