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: A4HHR2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.386 |
DEG_COP1_1 | 290 | 297 | PF00400 | 0.495 |
DOC_CDC14_PxL_1 | 255 | 263 | PF14671 | 0.352 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 347 | 354 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 87 | 95 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 292 | 299 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 242 | 245 | PF13499 | 0.288 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.512 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.290 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 391 | 399 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 436 | 440 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.687 |
LIG_Actin_WH2_2 | 383 | 399 | PF00022 | 0.517 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.317 |
LIG_CaM_IQ_9 | 222 | 238 | PF13499 | 0.511 |
LIG_DLG_GKlike_1 | 230 | 238 | PF00625 | 0.423 |
LIG_FAT_LD_1 | 48 | 56 | PF03623 | 0.562 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.505 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.419 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.355 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.437 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.479 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.511 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.444 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.415 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.556 |
LIG_GBD_Chelix_1 | 203 | 211 | PF00786 | 0.417 |
LIG_LIR_Gen_1 | 239 | 248 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 296 | 303 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.291 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.483 |
LIG_PDZ_Class_2 | 436 | 441 | PF00595 | 0.581 |
LIG_Pex14_1 | 431 | 435 | PF04695 | 0.386 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.481 |
LIG_SH2_GRB2like | 368 | 371 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.392 |
LIG_SH3_1 | 256 | 262 | PF00018 | 0.473 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.473 |
LIG_SUMO_SIM_par_1 | 110 | 116 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.486 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.295 |
LIG_TRAF2_1 | 61 | 64 | PF00917 | 0.588 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.329 |
LIG_TYR_ITIM | 402 | 407 | PF00017 | 0.289 |
LIG_Vh1_VBS_1 | 375 | 393 | PF01044 | 0.442 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.508 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.564 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.440 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.497 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.497 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.538 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.431 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.581 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.399 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.614 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.531 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.496 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.525 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.356 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.520 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.307 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.493 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.432 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.519 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.467 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.556 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.333 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.353 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.363 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.525 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.498 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.470 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.376 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.491 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.433 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.511 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.475 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.515 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.437 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.282 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.629 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.417 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.399 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.497 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.446 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.520 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.568 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.541 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.470 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.289 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.439 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.440 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.375 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.432 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.656 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.287 |
MOD_SUMO_rev_2 | 394 | 399 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 76 | 83 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.299 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y5 | Leptomonas seymouri | 50% | 96% |
A0A0S4IKI5 | Bodo saltans | 29% | 97% |
A0A1X0P918 | Trypanosomatidae | 37% | 95% |
A0A3Q8IFJ3 | Leishmania donovani | 79% | 100% |
A0A3R7K871 | Trypanosoma rangeli | 39% | 100% |
A4I4X2 | Leishmania infantum | 79% | 100% |
C9ZKY1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AEC6 | Leishmania major | 79% | 100% |
E9ALG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5BSL0 | Trypanosoma cruzi | 37% | 100% |