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: 2, no: 9 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4QB16
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.356 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.649 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.536 |
CLV_Separin_Metazoa | 134 | 138 | PF03568 | 0.310 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.460 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.665 |
DOC_MAPK_gen_1 | 335 | 343 | PF00069 | 0.655 |
DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.718 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.728 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.640 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.632 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 137 | 147 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.520 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.666 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.390 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.421 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.617 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.707 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.438 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.577 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.608 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.717 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.488 |
LIG_Integrin_isoDGR_2 | 286 | 288 | PF01839 | 0.446 |
LIG_LIR_Apic_2 | 256 | 260 | PF02991 | 0.697 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.702 |
LIG_LIR_Apic_2 | 31 | 36 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 107 | 115 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.390 |
LIG_NBox_RRM_1 | 216 | 226 | PF00076 | 0.449 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.673 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.703 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 289 | 293 | PF00017 | 0.625 |
LIG_SH2_STAT3 | 289 | 292 | PF00017 | 0.714 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.723 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.581 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.730 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.556 |
LIG_SH3_5 | 265 | 269 | PF00018 | 0.625 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.456 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.665 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.621 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.662 |
LIG_TRAF2_2 | 355 | 360 | PF00917 | 0.629 |
LIG_UBA3_1 | 55 | 63 | PF00899 | 0.524 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.684 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.441 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.496 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.508 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.756 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.718 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.699 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.376 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.667 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.585 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.735 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.719 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.456 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.775 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.544 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.735 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.645 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.545 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.748 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.704 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.708 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.489 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.546 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.650 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.400 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.476 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.355 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.470 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.621 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.609 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.477 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.535 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.604 |
MOD_PK_1 | 324 | 330 | PF00069 | 0.615 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.510 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.737 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.450 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.725 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.639 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.782 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.645 |
MOD_PKB_1 | 206 | 214 | PF00069 | 0.453 |
MOD_PKB_1 | 407 | 415 | PF00069 | 0.684 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.391 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.359 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.698 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.694 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.553 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.518 |
MOD_Plk_2-3 | 368 | 374 | PF00069 | 0.703 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.443 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.331 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.661 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.747 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.732 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.641 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.493 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.442 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.485 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.608 |
MOD_SUMO_for_1 | 130 | 133 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 114 | 124 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 327 | 336 | PF00179 | 0.669 |
TRG_DiLeu_BaEn_4 | 133 | 139 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_4 | 312 | 318 | PF01217 | 0.595 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S8 | Leptomonas seymouri | 65% | 98% |
A0A0S4IRC9 | Bodo saltans | 35% | 100% |
A0A1X0NWQ4 | Trypanosomatidae | 45% | 97% |
A0A3Q8IMB7 | Leishmania donovani | 94% | 100% |
A0A422NXY7 | Trypanosoma rangeli | 44% | 100% |
A4HD09 | Leishmania braziliensis | 77% | 100% |
A4I0J5 | Leishmania infantum | 94% | 100% |
C9ZVC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AWF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BJ93 | Trypanosoma cruzi | 43% | 99% |