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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0016020 | membrane | 2 | 10 |
Related structures:
AlphaFold database: Q4Q3Q0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.441 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.335 |
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.267 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.536 |
CLV_PCSK_FUR_1 | 41 | 45 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.608 |
DOC_CKS1_1 | 162 | 167 | PF01111 | 0.387 |
DOC_CYCLIN_RxL_1 | 381 | 393 | PF00134 | 0.389 |
DOC_MAPK_FxFP_2 | 6 | 9 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 121 | 130 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 358 | 366 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 385 | 392 | PF00069 | 0.331 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.449 |
DOC_PP2B_PxIxI_1 | 125 | 131 | PF00149 | 0.329 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.609 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.558 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.221 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 236 | 244 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.208 |
LIG_Actin_WH2_2 | 137 | 154 | PF00022 | 0.469 |
LIG_Clathr_ClatBox_1 | 389 | 393 | PF01394 | 0.325 |
LIG_deltaCOP1_diTrp_1 | 368 | 376 | PF00928 | 0.361 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.471 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.466 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.411 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.286 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.210 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.572 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.484 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.440 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.338 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.279 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.373 |
LIG_HP1_1 | 388 | 392 | PF01393 | 0.331 |
LIG_IBAR_NPY_1 | 378 | 380 | PF08397 | 0.341 |
LIG_LIR_Apic_2 | 373 | 379 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.316 |
LIG_LIR_LC3C_4 | 137 | 142 | PF02991 | 0.329 |
LIG_LIR_LC3C_4 | 386 | 391 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.406 |
LIG_NBox_RRM_1 | 264 | 274 | PF00076 | 0.221 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.490 |
LIG_Pex14_1 | 376 | 380 | PF04695 | 0.371 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.553 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.574 |
LIG_SH2_GRB2like | 200 | 203 | PF00017 | 0.358 |
LIG_SH2_GRB2like | 380 | 383 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 177 | 180 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.391 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.482 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.407 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.296 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.456 |
LIG_SUMO_SIM_par_1 | 386 | 394 | PF11976 | 0.332 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.551 |
LIG_TYR_ITIM | 141 | 146 | PF00017 | 0.614 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.573 |
MOD_CDK_SPK_2 | 351 | 356 | PF00069 | 0.221 |
MOD_CDK_SPxxK_3 | 351 | 358 | PF00069 | 0.221 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.445 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.694 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.671 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.562 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.481 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.261 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.470 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.550 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.466 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.519 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.391 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.784 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.396 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.431 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.786 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.500 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.579 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.455 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.361 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.313 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.575 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.647 |
MOD_OFUCOSY | 203 | 208 | PF10250 | 0.541 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.377 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.248 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.208 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.579 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.388 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.285 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.439 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.411 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.616 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.337 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.326 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.651 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.601 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.485 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.460 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.281 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.221 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.353 |
TRG_DiLeu_BaLyEn_6 | 101 | 106 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.615 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB04 | Leptomonas seymouri | 57% | 100% |
A0A1X0NR96 | Trypanosomatidae | 44% | 100% |
A0A3S5IRC8 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WZA9 | Leishmania donovani | 28% | 100% |
A0A3S7X774 | Leishmania donovani | 86% | 100% |
A4HLZ4 | Leishmania braziliensis | 34% | 96% |
A4HLZ6 | Leishmania braziliensis | 69% | 100% |
A4I1M7 | Leishmania infantum | 28% | 100% |
A4I9C6 | Leishmania infantum | 86% | 100% |
E9AXR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B4C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q9R0 | Leishmania major | 29% | 100% |