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: A0A3S7X164
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.558 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.491 |
DEG_SCF_FBW7_1 | 252 | 259 | PF00400 | 0.752 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.565 |
DOC_MAPK_DCC_7 | 378 | 388 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 276 | 285 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 412 | 420 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 313 | 320 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 380 | 388 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 105 | 111 | PF00149 | 0.459 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.765 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.506 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.492 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.568 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.374 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.526 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.429 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.500 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.350 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.772 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.533 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.559 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.777 |
LIG_LIR_Apic_2 | 184 | 188 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 109 | 117 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 325 | 332 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.468 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 185 | 189 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.432 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.525 |
LIG_SH3_4 | 410 | 417 | PF00018 | 0.535 |
LIG_SH3_4 | 50 | 57 | PF00018 | 0.512 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.469 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.581 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.675 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.678 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.477 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.467 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.566 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.498 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.494 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.511 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.502 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.719 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.408 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.579 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.493 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.473 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.500 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.453 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.441 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.772 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.718 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.296 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.396 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.395 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.492 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.527 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.466 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.762 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.296 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.469 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.365 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.552 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.548 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.527 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.415 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.502 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.453 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.397 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.544 |
MOD_NEK2_2 | 349 | 354 | PF00069 | 0.519 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.516 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.454 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.543 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.735 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.540 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.562 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.487 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.718 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.535 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.415 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.478 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.411 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.465 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.536 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.561 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.776 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 243 | 249 | PF00179 | 0.789 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.649 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.397 |
TRG_NES_CRM1_1 | 390 | 403 | PF08389 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJS3 | Leptomonas seymouri | 53% | 100% |
A0A0S4KFQ7 | Bodo saltans | 27% | 100% |
A0A1X0NYM7 | Trypanosomatidae | 30% | 87% |
A0A3R7KQG6 | Trypanosoma rangeli | 38% | 95% |
A4I3A5 | Leishmania infantum | 99% | 100% |
D0A828 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AZK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q8M8 | Leishmania major | 91% | 100% |
V5B0U4 | Trypanosoma cruzi | 34% | 90% |