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: 6, no: 0 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HGX2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.417 |
CLV_MEL_PAP_1 | 139 | 145 | PF00089 | 0.599 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.670 |
DEG_APCC_DBOX_1 | 347 | 355 | PF00400 | 0.700 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.427 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.558 |
DOC_MAPK_gen_1 | 3 | 13 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.414 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.739 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.681 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 227 | 236 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 348 | 356 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.704 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.727 |
LIG_deltaCOP1_diTrp_1 | 131 | 138 | PF00928 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 46 | 52 | PF00928 | 0.497 |
LIG_EH1_1 | 9 | 17 | PF00400 | 0.402 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.382 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.474 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.517 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.303 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.532 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 377 | 383 | PF02991 | 0.733 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.421 |
LIG_NRBOX | 135 | 141 | PF00104 | 0.393 |
LIG_Pex14_1 | 155 | 159 | PF04695 | 0.406 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.471 |
LIG_SH2_GRB2like | 287 | 290 | PF00017 | 0.319 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 151 | 154 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.704 |
LIG_SH3_1 | 368 | 374 | PF00018 | 0.710 |
LIG_SH3_2 | 371 | 376 | PF14604 | 0.712 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.451 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.686 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.665 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.450 |
LIG_SUMO_SIM_par_1 | 18 | 25 | PF11976 | 0.498 |
LIG_UBA3_1 | 327 | 333 | PF00899 | 0.474 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.471 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.497 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.494 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.406 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.309 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.566 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.238 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.494 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.583 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.391 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.399 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.345 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.629 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.616 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.569 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.682 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.587 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.614 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.559 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.673 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.546 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.476 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.475 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.474 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.368 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.322 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.556 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.471 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.780 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.663 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.670 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.608 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.696 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.424 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.498 |
MOD_N-GLC_2 | 261 | 263 | PF02516 | 0.526 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.427 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.402 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.505 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.335 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.520 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.538 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.747 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.786 |
MOD_NEK2_2 | 132 | 137 | PF00069 | 0.390 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.356 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.437 |
MOD_PKB_1 | 358 | 366 | PF00069 | 0.706 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.699 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.440 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.506 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.696 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.513 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.456 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.471 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.704 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.807 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3M3 | Leptomonas seymouri | 46% | 100% |
A0A3S7X1V5 | Leishmania donovani | 70% | 100% |
A4I402 | Leishmania infantum | 70% | 100% |
E9B092 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q7Z3 | Leishmania major | 66% | 92% |