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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4QIL2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.765 |
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.411 |
DEG_COP1_1 | 138 | 148 | PF00400 | 0.685 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.684 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.783 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.789 |
DOC_CYCLIN_RxL_1 | 153 | 164 | PF00134 | 0.615 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.389 |
DOC_PP1_RVXF_1 | 317 | 323 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.523 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 319 | 323 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.504 |
LIG_CSL_BTD_1 | 347 | 350 | PF09270 | 0.523 |
LIG_EH1_1 | 354 | 362 | PF00400 | 0.459 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.738 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.684 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.557 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.523 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.447 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.761 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.616 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.609 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.708 |
LIG_GBD_Chelix_1 | 372 | 380 | PF00786 | 0.447 |
LIG_HP1_1 | 16 | 20 | PF01393 | 0.675 |
LIG_LIR_Apic_2 | 345 | 351 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 354 | 361 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 153 | 158 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.504 |
LIG_Pex14_1 | 274 | 278 | PF04695 | 0.487 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.653 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.639 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 67 | 71 | PF00017 | 0.746 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.639 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.746 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.752 |
LIG_SUMO_SIM_anti_2 | 15 | 22 | PF11976 | 0.675 |
LIG_SUMO_SIM_par_1 | 15 | 22 | PF11976 | 0.675 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.790 |
LIG_TYR_ITIM | 335 | 340 | PF00017 | 0.529 |
LIG_WRC_WIRS_1 | 145 | 150 | PF05994 | 0.620 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.673 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.733 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.760 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.713 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.679 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.714 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.641 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.717 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.715 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.776 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.635 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.613 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.713 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.452 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.457 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.510 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.450 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.447 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.749 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.767 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.465 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.474 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.541 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.541 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.527 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.542 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.445 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.767 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.734 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.651 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.561 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.531 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.629 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.706 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.726 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.441 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.776 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.714 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.524 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.452 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.740 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.739 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.732 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.713 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.569 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.641 |
MOD_Plk_2-3 | 128 | 134 | PF00069 | 0.774 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.740 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.447 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.781 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.754 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.484 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.664 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.737 |
MOD_SUMO_rev_2 | 128 | 136 | PF00179 | 0.793 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.659 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.655 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.525 |
TRG_NES_CRM1_1 | 150 | 164 | PF08389 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPX9 | Leishmania donovani | 90% | 96% |
A4H529 | Leishmania braziliensis | 71% | 77% |
A4HTA3 | Leishmania infantum | 90% | 66% |
E9AL92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |