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: A4IB65
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.444 |
DEG_SCF_TRCP1_1 | 25 | 31 | PF00400 | 0.535 |
DOC_MIT_MIM_1 | 347 | 356 | PF04212 | 0.467 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.580 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 320 | 328 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.796 |
LIG_Actin_WH2_2 | 293 | 309 | PF00022 | 0.566 |
LIG_APCC_ABBA_1 | 265 | 270 | PF00400 | 0.424 |
LIG_EH1_1 | 240 | 248 | PF00400 | 0.495 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.611 |
LIG_LIR_Apic_2 | 142 | 147 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.550 |
LIG_LYPXL_S_1 | 265 | 269 | PF13949 | 0.365 |
LIG_MAD2 | 4 | 12 | PF02301 | 0.614 |
LIG_NRBOX | 212 | 218 | PF00104 | 0.522 |
LIG_PDZ_Class_3 | 351 | 356 | PF00595 | 0.516 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.537 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 283 | 286 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.494 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.628 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.620 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.751 |
LIG_WW_1 | 146 | 149 | PF00397 | 0.656 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.476 |
MOD_CDK_SPxxK_3 | 75 | 82 | PF00069 | 0.553 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.563 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.626 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.472 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.521 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.620 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.688 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.718 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.415 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.682 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.544 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.656 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.665 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.635 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.459 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.689 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.681 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.736 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.617 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.560 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.622 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.596 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.559 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.650 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.455 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.592 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.568 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.534 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.674 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.480 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.591 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.700 |
MOD_SUMO_rev_2 | 99 | 108 | PF00179 | 0.553 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 212 | 217 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKF7 | Leptomonas seymouri | 36% | 100% |
A0A3S7X929 | Leishmania donovani | 99% | 100% |
A4HMI5 | Leishmania braziliensis | 72% | 100% |
E9AEY6 | Leishmania major | 90% | 100% |
E9B642 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |