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: Q4QBB5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.652 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.563 |
DEG_SCF_FBW7_1 | 131 | 136 | PF00400 | 0.698 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.728 |
DOC_ANK_TNKS_1 | 226 | 233 | PF00023 | 0.800 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.695 |
DOC_CYCLIN_RxL_1 | 205 | 217 | PF00134 | 0.716 |
DOC_CYCLIN_RxL_1 | 301 | 312 | PF00134 | 0.686 |
DOC_CYCLIN_RxL_1 | 355 | 365 | PF00134 | 0.581 |
DOC_PP1_RVXF_1 | 302 | 309 | PF00149 | 0.735 |
DOC_PP1_RVXF_1 | 355 | 362 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.570 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.716 |
DOC_USP7_MATH_2 | 221 | 227 | PF00917 | 0.825 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.642 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.705 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.592 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.542 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.669 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.780 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.536 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.514 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.836 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.734 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.670 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.514 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.447 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.720 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.498 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 319 | 328 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.747 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.590 |
LIG_SH2_PTP2 | 322 | 325 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.526 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.609 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.776 |
LIG_SH3_5 | 196 | 200 | PF00018 | 0.611 |
LIG_SUMO_SIM_par_1 | 209 | 217 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.751 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.661 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.744 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.592 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.666 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.596 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.771 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.769 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.811 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.699 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.773 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.689 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.481 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.717 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.719 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.570 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.565 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.677 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.508 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.672 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.718 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.746 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.777 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.775 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.731 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.714 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.775 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.628 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.693 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.520 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.683 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.813 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.573 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.685 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.726 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.693 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.632 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.613 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.573 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.716 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.752 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.494 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.697 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.700 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.509 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.747 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.760 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.663 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.736 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.630 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.698 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.738 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.573 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.712 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.508 |
MOD_Plk_2-3 | 294 | 300 | PF00069 | 0.714 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.757 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.684 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.690 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.592 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.453 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.508 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.667 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.651 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.697 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.539 |
MOD_SUMO_rev_2 | 215 | 221 | PF00179 | 0.810 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.746 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.812 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 60 | 64 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE95 | Leptomonas seymouri | 48% | 94% |
A0A3S5H7B8 | Leishmania donovani | 88% | 100% |
A4HCS4 | Leishmania braziliensis | 78% | 100% |
A4I098 | Leishmania infantum | 87% | 80% |
E9AW63 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |