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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q395
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.563 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.494 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.489 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.528 |
DEG_SCF_FBW7_2 | 257 | 263 | PF00400 | 0.540 |
DOC_CKS1_1 | 257 | 262 | PF01111 | 0.538 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.418 |
DOC_CKS1_1 | 53 | 58 | PF01111 | 0.584 |
DOC_CYCLIN_RxL_1 | 329 | 336 | PF00134 | 0.493 |
DOC_CYCLIN_RxL_1 | 37 | 46 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 296 | 302 | PF00069 | 0.615 |
DOC_MAPK_gen_1 | 312 | 320 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 360 | 367 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 39 | 45 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 314 | 326 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 317 | 326 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 78 | 85 | PF00069 | 0.589 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.584 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.511 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.517 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.491 |
LIG_deltaCOP1_diTrp_1 | 5 | 11 | PF00928 | 0.479 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.623 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.482 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.453 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.556 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.677 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.375 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.480 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.462 |
LIG_GBD_Chelix_1 | 330 | 338 | PF00786 | 0.501 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.539 |
LIG_MAD2 | 40 | 48 | PF02301 | 0.531 |
LIG_NRBOX | 165 | 171 | PF00104 | 0.465 |
LIG_PCNA_yPIPBox_3 | 364 | 378 | PF02747 | 0.496 |
LIG_Pex14_2 | 335 | 339 | PF04695 | 0.424 |
LIG_Pex14_2 | 353 | 357 | PF04695 | 0.394 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.629 |
LIG_SH3_1 | 305 | 311 | PF00018 | 0.535 |
LIG_SH3_2 | 308 | 313 | PF14604 | 0.550 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.550 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.546 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.535 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.527 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.528 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.629 |
LIG_SUMO_SIM_par_1 | 41 | 46 | PF11976 | 0.516 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.653 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.539 |
MOD_CDC14_SPxK_1 | 249 | 252 | PF00782 | 0.602 |
MOD_CDK_SPxK_1 | 246 | 252 | PF00069 | 0.598 |
MOD_CDK_SPxxK_3 | 246 | 253 | PF00069 | 0.551 |
MOD_CDK_SPxxK_3 | 325 | 332 | PF00069 | 0.502 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.636 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.608 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.729 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.566 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.494 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.630 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.591 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.495 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.544 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.385 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.478 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.463 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.587 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.654 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.646 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.484 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.517 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.549 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.607 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.657 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.585 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.571 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.553 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.431 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.527 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.627 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.532 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.657 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.592 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.644 |
MOD_LATS_1 | 120 | 126 | PF00433 | 0.608 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.638 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.553 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.415 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.417 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.471 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.535 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.593 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.604 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.538 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.629 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.705 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.615 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.538 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.652 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.679 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.478 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.474 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.592 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.483 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.573 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.402 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.496 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.461 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.506 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.591 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.662 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.493 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.623 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.573 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.428 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.608 |
MOD_SUMO_rev_2 | 88 | 96 | PF00179 | 0.667 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.539 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P9L5 | Trypanosomatidae | 24% | 94% |
A0A3Q8II07 | Leishmania donovani | 89% | 99% |
A4HAM8 | Leishmania braziliensis | 68% | 96% |
A4I9S0 | Leishmania infantum | 90% | 69% |
E9B4T1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |