Uncharacterized Protein, Uncharacterized
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: A4HZM7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.342 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.492 |
DEG_SPOP_SBC_1 | 278 | 282 | PF00917 | 0.612 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.427 |
DOC_MAPK_gen_1 | 10 | 20 | PF00069 | 0.452 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.398 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.416 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 262 | 266 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 288 | 298 | PF00244 | 0.726 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.421 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.477 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.780 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.482 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.342 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.754 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.560 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.331 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.341 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.495 |
LIG_LIR_Apic_2 | 226 | 230 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 32 | 38 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 164 | 172 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 363 | 372 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 363 | 367 | PF02991 | 0.317 |
LIG_Pex14_1 | 227 | 231 | PF04695 | 0.395 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.501 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 364 | 367 | PF00017 | 0.306 |
LIG_SH2_SRC | 250 | 253 | PF00017 | 0.357 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.365 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.505 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.401 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.315 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.229 |
LIG_SUMO_SIM_anti_2 | 131 | 137 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 324 | 334 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 339 | 344 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 324 | 334 | PF11976 | 0.342 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.394 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.306 |
LIG_UBA3_1 | 247 | 256 | PF00899 | 0.398 |
MOD_CDK_SPK_2 | 257 | 262 | PF00069 | 0.455 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.468 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.651 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.712 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.636 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.348 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.519 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.453 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.440 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.657 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.342 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.394 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.458 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.377 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.649 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.654 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.616 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.551 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.562 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.443 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.526 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.421 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.509 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.623 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.547 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.666 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.313 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.474 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.348 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.593 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.589 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.408 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.288 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.642 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.331 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.409 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.583 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.465 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.419 |
MOD_PK_1 | 24 | 30 | PF00069 | 0.417 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.620 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.465 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.494 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.636 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.316 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.244 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.451 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.453 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.477 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.351 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.444 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.348 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.348 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.436 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.511 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.572 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.729 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.440 |
MOD_SUMO_for_1 | 360 | 363 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 171 | 175 | PF00179 | 0.439 |
MOD_SUMO_rev_2 | 350 | 356 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 377 | 383 | PF00179 | 0.308 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.500 |
TRG_ER_diLys_1 | 381 | 384 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 339 | 352 | PF08389 | 0.296 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3J1 | Leptomonas seymouri | 35% | 100% |
A0A0N0P3Y3 | Leptomonas seymouri | 61% | 100% |
A0A3Q8IAB9 | Leishmania donovani | 99% | 100% |
A0A3Q8IF47 | Leishmania donovani | 35% | 100% |
A4HZM6 | Leishmania infantum | 35% | 94% |
E9AV54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 96% |
E9AV55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 94% |
Q4QCC6 | Leishmania major | 34% | 91% |
Q4QCC7 | Leishmania major | 94% | 100% |