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 |
Related structures:
AlphaFold database: A4H962
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.395 |
DEG_SCF_FBW7_1 | 438 | 445 | PF00400 | 0.548 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.629 |
DOC_CYCLIN_RxL_1 | 127 | 135 | PF00134 | 0.777 |
DOC_CYCLIN_yCln2_LP_2 | 279 | 285 | PF00134 | 0.660 |
DOC_MAPK_gen_1 | 127 | 133 | PF00069 | 0.775 |
DOC_MAPK_gen_1 | 263 | 271 | PF00069 | 0.697 |
DOC_PP1_RVXF_1 | 128 | 134 | PF00149 | 0.743 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.642 |
DOC_PP2B_LxvP_1 | 167 | 170 | PF13499 | 0.686 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.509 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 311 | 319 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 65 | 72 | PF00244 | 0.678 |
LIG_APCC_ABBA_1 | 269 | 274 | PF00400 | 0.641 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.761 |
LIG_deltaCOP1_diTrp_1 | 88 | 95 | PF00928 | 0.651 |
LIG_eIF4E_1 | 39 | 45 | PF01652 | 0.621 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.722 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.619 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.564 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.430 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.314 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.621 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.569 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.621 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.700 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.633 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.366 |
LIG_LIR_Apic_2 | 228 | 234 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.774 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.726 |
LIG_LYPXL_yS_3 | 164 | 167 | PF13949 | 0.662 |
LIG_PDZ_Class_2 | 447 | 452 | PF00595 | 0.590 |
LIG_Pex14_1 | 189 | 193 | PF04695 | 0.752 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.658 |
LIG_PTB_Apo_2 | 171 | 178 | PF02174 | 0.671 |
LIG_PTB_Apo_2 | 33 | 40 | PF02174 | 0.749 |
LIG_PTB_Phospho_1 | 171 | 177 | PF10480 | 0.667 |
LIG_PTB_Phospho_1 | 33 | 39 | PF10480 | 0.616 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.693 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.724 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.411 |
LIG_SH3_2 | 208 | 213 | PF14604 | 0.654 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.671 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.367 |
LIG_SUMO_SIM_anti_2 | 417 | 422 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.366 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.700 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.595 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.566 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.622 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.678 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.715 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.630 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.763 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.741 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.507 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.509 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.794 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.621 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.774 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.600 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.512 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.612 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.547 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.494 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.708 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.536 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.559 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.498 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.688 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.740 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.727 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.793 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.327 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.411 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.602 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.411 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.578 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.509 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.588 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.796 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.471 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.357 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.800 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.597 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.720 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.714 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.558 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.628 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.691 |
TRG_DiLeu_BaEn_2 | 303 | 309 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.692 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.183 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D5 | Leptomonas seymouri | 49% | 72% |
A0A3Q8IAR6 | Leishmania donovani | 64% | 86% |
A4HXI4 | Leishmania infantum | 64% | 86% |
E9AR79 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 98% |
Q4QE84 | Leishmania major | 61% | 100% |