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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HMP7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.520 |
CLV_PCSK_FUR_1 | 432 | 436 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.612 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.502 |
DOC_ANK_TNKS_1 | 155 | 162 | PF00023 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 203 | 209 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.668 |
DOC_MAPK_FxFP_2 | 326 | 329 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 242 | 252 | PF00069 | 0.405 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.619 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.412 |
DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.286 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 333 | 342 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 35 | 43 | PF00244 | 0.695 |
LIG_Actin_WH2_2 | 304 | 320 | PF00022 | 0.487 |
LIG_BIR_III_2 | 385 | 389 | PF00653 | 0.396 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.497 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.525 |
LIG_CSL_BTD_1 | 425 | 428 | PF09270 | 0.587 |
LIG_EH1_1 | 246 | 254 | PF00400 | 0.360 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.689 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.571 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.502 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.462 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.476 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 228 | 234 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 27 | 34 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 366 | 376 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 394 | 405 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.377 |
LIG_PDZ_Class_3 | 436 | 441 | PF00595 | 0.453 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.511 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 274 | 277 | PF00017 | 0.291 |
LIG_SH2_SRC | 274 | 277 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.260 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.498 |
LIG_SH3_1 | 124 | 130 | PF00018 | 0.279 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.368 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.323 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.406 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.547 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.724 |
LIG_SUMO_SIM_anti_2 | 213 | 219 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.343 |
LIG_SxIP_EBH_1 | 131 | 143 | PF03271 | 0.299 |
LIG_TRFH_1 | 340 | 344 | PF08558 | 0.547 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.447 |
MOD_CDK_SPK_2 | 39 | 44 | PF00069 | 0.550 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.405 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.649 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.626 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.528 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.516 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.331 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.720 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.352 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.441 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.715 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.654 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.649 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.336 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.538 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.456 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.718 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.609 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.571 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.336 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.412 |
MOD_N-GLC_2 | 103 | 105 | PF02516 | 0.257 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.602 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.344 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.297 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.615 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.480 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.248 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.597 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.450 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.450 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.473 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.620 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.643 |
MOD_PKB_1 | 332 | 340 | PF00069 | 0.525 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.565 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.572 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.345 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.409 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.474 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.777 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.366 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.681 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.448 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.624 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.629 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.631 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.516 |
TRG_NLS_MonoExtN_4 | 139 | 144 | PF00514 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 295 | 300 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3L8 | Leptomonas seymouri | 45% | 81% |
A0A0S4JDL6 | Bodo saltans | 28% | 100% |
A0A1X0P5V1 | Trypanosomatidae | 43% | 100% |
A0A3Q8IJ19 | Leishmania donovani | 75% | 83% |
A0A422NLY6 | Trypanosoma rangeli | 40% | 100% |
A4IBB6 | Leishmania infantum | 75% | 83% |
C9ZZD3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AF48 | Leishmania major | 73% | 100% |
E9B6A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 85% |
V5DKB8 | Trypanosoma cruzi | 40% | 100% |