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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QGE8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.526 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.512 |
CLV_PCSK_FUR_1 | 90 | 94 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 322 | 326 | PF03568 | 0.625 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.508 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.645 |
DOC_CYCLIN_RxL_1 | 17 | 26 | PF00134 | 0.674 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 376 | 385 | PF00134 | 0.653 |
DOC_MAPK_gen_1 | 219 | 229 | PF00069 | 0.646 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 350 | 359 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.626 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.672 |
DOC_PP4_MxPP_1 | 11 | 14 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 303 | 309 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.646 |
LIG_Actin_WH2_2 | 309 | 327 | PF00022 | 0.623 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.634 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.673 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.639 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.636 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.484 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.684 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.581 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.597 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.717 |
LIG_Integrin_RGD_1 | 212 | 214 | PF01839 | 0.698 |
LIG_LIR_Apic_2 | 307 | 312 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 143 | 152 | PF02991 | 0.751 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.743 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.475 |
LIG_PAM2_1 | 252 | 264 | PF00658 | 0.533 |
LIG_PCNA_yPIPBox_3 | 73 | 87 | PF02747 | 0.545 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.580 |
LIG_SH2_CRK | 309 | 313 | PF00017 | 0.492 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.658 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.709 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.484 |
LIG_SUMO_SIM_anti_2 | 358 | 365 | PF11976 | 0.650 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.616 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.621 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.703 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.613 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.645 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.691 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.676 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.544 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.683 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.577 |
MOD_DYRK1A_RPxSP_1 | 12 | 16 | PF00069 | 0.730 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.662 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.518 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.766 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.642 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.526 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.560 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.542 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.616 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.752 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.468 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.631 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.566 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.568 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.696 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.518 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.684 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.673 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.614 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.745 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.657 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.616 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.617 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.530 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.688 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.671 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.652 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.654 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.711 |
MOD_PKA_1 | 263 | 269 | PF00069 | 0.563 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.687 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.679 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.638 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.677 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.569 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.540 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.620 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.678 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.693 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.667 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.675 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.651 |
MOD_SUMO_rev_2 | 346 | 352 | PF00179 | 0.737 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.554 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.691 |
TRG_DiLeu_LyEn_5 | 371 | 376 | PF01217 | 0.594 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.604 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1S5 | Leptomonas seymouri | 44% | 86% |
A0A1X0NNN8 | Trypanosomatidae | 24% | 72% |
A0A3R7MBM6 | Trypanosoma rangeli | 24% | 76% |
A0A3S5H6M8 | Leishmania donovani | 90% | 71% |
A4H714 | Leishmania braziliensis | 72% | 85% |
A4HVE2 | Leishmania infantum | 89% | 71% |
E9AP40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |