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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AEE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.635 |
CLV_MEL_PAP_1 | 193 | 199 | PF00089 | 0.562 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.397 |
DOC_ANK_TNKS_1 | 8 | 15 | PF00023 | 0.454 |
DOC_CYCLIN_RxL_1 | 2 | 11 | PF00134 | 0.664 |
DOC_CYCLIN_yCln2_LP_2 | 149 | 155 | PF00134 | 0.521 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 278 | 281 | PF13499 | 0.355 |
DOC_PP2B_PxIxI_1 | 95 | 101 | PF00149 | 0.442 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.508 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 208 | 212 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.634 |
LIG_Actin_WH2_2 | 109 | 124 | PF00022 | 0.544 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.622 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.502 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.332 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.400 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.420 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.574 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.505 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.376 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.529 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.414 |
LIG_LIR_Apic_2 | 34 | 40 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 230 | 237 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 271 | 282 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.398 |
LIG_MYND_1 | 348 | 352 | PF01753 | 0.617 |
LIG_PDZ_Class_3 | 380 | 385 | PF00595 | 0.594 |
LIG_Pex14_1 | 125 | 129 | PF04695 | 0.400 |
LIG_Rb_pABgroove_1 | 300 | 308 | PF01858 | 0.297 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.404 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.480 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.369 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.305 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.371 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.477 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.573 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.433 |
LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 334 | 341 | PF11976 | 0.401 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.302 |
LIG_UBA3_1 | 359 | 366 | PF00899 | 0.516 |
MOD_CDK_SPxxK_3 | 92 | 99 | PF00069 | 0.545 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.474 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.487 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.547 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.503 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.547 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.277 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.451 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.686 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.433 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.543 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.559 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.570 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.569 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.581 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.543 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.347 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.395 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.528 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.622 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.605 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.418 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.575 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.496 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.659 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.514 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.523 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.448 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.562 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.335 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.712 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.500 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.462 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.642 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.488 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.562 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.498 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.362 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.487 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.665 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.487 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.544 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.550 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.386 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.704 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.398 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.453 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.413 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.596 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IG75 | Leptomonas seymouri | 52% | 100% |
A0A0S4J6P5 | Bodo saltans | 25% | 90% |
A0A1X0PAK7 | Trypanosomatidae | 38% | 100% |
A0A3S5H7M1 | Leishmania donovani | 88% | 100% |
A0A422NJ09 | Trypanosoma rangeli | 36% | 100% |
A4H3R2 | Leishmania braziliensis | 70% | 100% |
A4I4Y1 | Leishmania infantum | 88% | 100% |
C9ZLM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9ALD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5B889 | Trypanosoma cruzi | 39% | 93% |