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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QJ43
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.429 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.524 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 239 | 245 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 196 | 204 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 395 | 401 | PF00069 | 0.726 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 379 | 382 | PF13499 | 0.699 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 407 | 417 | PF00244 | 0.745 |
LIG_Actin_WH2_2 | 139 | 156 | PF00022 | 0.552 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.589 |
LIG_Clathr_ClatBox_1 | 436 | 440 | PF01394 | 0.678 |
LIG_deltaCOP1_diTrp_1 | 212 | 219 | PF00928 | 0.549 |
LIG_DLG_GKlike_1 | 260 | 267 | PF00625 | 0.504 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.491 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.659 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.747 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.662 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.700 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.628 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.690 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.624 |
LIG_GBD_Chelix_1 | 88 | 96 | PF00786 | 0.668 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 263 | 272 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 367 | 374 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.623 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.507 |
LIG_PDZ_Class_3 | 446 | 451 | PF00595 | 0.678 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 161 | 164 | PF00017 | 0.416 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.625 |
LIG_Sin3_1 | 223 | 233 | PF02671 | 0.474 |
LIG_SUMO_SIM_par_1 | 251 | 258 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 269 | 276 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 431 | 440 | PF11976 | 0.699 |
LIG_TYR_ITIM | 262 | 267 | PF00017 | 0.421 |
LIG_UBA3_1 | 92 | 101 | PF00899 | 0.537 |
LIG_WRC_WIRS_1 | 174 | 179 | PF05994 | 0.512 |
MOD_CDK_SPxK_1 | 80 | 86 | PF00069 | 0.428 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.600 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.477 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.602 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.690 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.671 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.591 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.687 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.640 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.497 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.583 |
MOD_Cter_Amidation | 258 | 261 | PF01082 | 0.558 |
MOD_Cter_Amidation | 331 | 334 | PF01082 | 0.740 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.484 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.464 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.522 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.676 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.516 |
MOD_GlcNHglycan | 323 | 327 | PF01048 | 0.434 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.585 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.659 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.742 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.477 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.599 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.418 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.630 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.484 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.514 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.423 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.494 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.463 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.363 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.711 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.621 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.500 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.644 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.517 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.461 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.463 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.457 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.556 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.676 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.598 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.516 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.560 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.566 |
MOD_OFUCOSY | 105 | 112 | PF10250 | 0.706 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.734 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.505 |
MOD_PKA_1 | 403 | 409 | PF00069 | 0.673 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.471 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.507 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.627 |
MOD_PKB_1 | 405 | 413 | PF00069 | 0.663 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.498 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.497 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.478 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.586 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.443 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.229 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.554 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.570 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.555 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.428 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 325 | 335 | PF00179 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.650 |
TRG_NLS_MonoExtC_3 | 402 | 407 | PF00514 | 0.652 |
TRG_NLS_MonoExtN_4 | 403 | 408 | PF00514 | 0.721 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZQ7 | Leptomonas seymouri | 46% | 100% |
A0A1X0NL47 | Trypanosomatidae | 33% | 98% |
A0A3S5H5P7 | Leishmania donovani | 95% | 100% |
A0A3S5IR10 | Trypanosoma rangeli | 30% | 97% |
A4H4K1 | Leishmania braziliensis | 78% | 100% |
A4HSS7 | Leishmania infantum | 95% | 100% |
C9ZTC6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 98% |
E9AKR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BA95 | Trypanosoma cruzi | 32% | 98% |