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: E9ARI7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.661 |
CLV_PCSK_PC7_1 | 413 | 419 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.471 |
CLV_Separin_Metazoa | 293 | 297 | PF03568 | 0.494 |
DEG_SCF_TRCP1_1 | 55 | 61 | PF00400 | 0.502 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 107 | 114 | PF00069 | 0.584 |
DOC_PP1_RVXF_1 | 91 | 97 | PF00149 | 0.611 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.666 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.419 |
LIG_deltaCOP1_diTrp_1 | 139 | 147 | PF00928 | 0.487 |
LIG_deltaCOP1_diTrp_1 | 249 | 256 | PF00928 | 0.427 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.270 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.362 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.485 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.454 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.611 |
LIG_LIR_Gen_1 | 210 | 220 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 273 | 279 | PF02991 | 0.195 |
LIG_LIR_Gen_1 | 364 | 372 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 397 | 406 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 364 | 368 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.404 |
LIG_PCNA_PIPBox_1 | 22 | 31 | PF02747 | 0.484 |
LIG_PCNA_yPIPBox_3 | 15 | 29 | PF02747 | 0.484 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.483 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.360 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.495 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.573 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.474 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.461 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 402 | 408 | PF11976 | 0.517 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.477 |
LIG_TYR_ITIM | 363 | 368 | PF00017 | 0.362 |
LIG_UBA3_1 | 368 | 377 | PF00899 | 0.372 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.692 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.407 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.551 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.441 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.642 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.698 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.533 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.483 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.231 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.720 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.551 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.656 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.574 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.392 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.609 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.568 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.391 |
MOD_GlcNHglycan | 244 | 248 | PF01048 | 0.561 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.410 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.552 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.669 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.667 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.470 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.699 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.672 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.575 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.417 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.463 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.636 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.475 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.698 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.666 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.546 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.501 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.684 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.439 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.395 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.554 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.563 |
MOD_PKA_1 | 107 | 113 | PF00069 | 0.710 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.564 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.412 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.762 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.505 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.497 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.542 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.420 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.362 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.516 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.643 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.604 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.429 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.665 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.510 |
TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.489 |
TRG_NLS_MonoExtC_3 | 412 | 417 | PF00514 | 0.472 |
TRG_NLS_MonoExtN_4 | 27 | 34 | PF00514 | 0.376 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5D0 | Leptomonas seymouri | 53% | 98% |
A0A0S4JE52 | Bodo saltans | 26% | 100% |
A0A1X0P6Z6 | Trypanosomatidae | 38% | 100% |
A0A3Q8IB26 | Leishmania donovani | 91% | 100% |
A0A422NJ49 | Trypanosoma rangeli | 40% | 100% |
A4H9F8 | Leishmania braziliensis | 77% | 100% |
A4HXS5 | Leishmania infantum | 91% | 100% |
D0A057 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4QDZ2 | Leishmania major | 90% | 100% |
V5BRN6 | Trypanosoma cruzi | 35% | 100% |