This protein family is endemic to Kinetoplastids, might have emerged de novo and also expanded. . The family also contains Leishmaniid members lacking the signal peptide and only having an MTTPA- start sequence
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 | yes | yes: 2, no: 9 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4H5C6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.344 |
DEG_MDM2_SWIB_1 | 93 | 101 | PF02201 | 0.426 |
DOC_MAPK_gen_1 | 36 | 42 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.251 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.398 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.368 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.747 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.508 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.464 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.349 |
LIG_eIF4E_1 | 98 | 104 | PF01652 | 0.365 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.327 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.578 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.444 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.449 |
LIG_REV1ctd_RIR_1 | 90 | 98 | PF16727 | 0.351 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.619 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.451 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.394 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.633 |
LIG_SH2_STAT3 | 126 | 129 | PF00017 | 0.619 |
LIG_SH2_STAT3 | 80 | 83 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.523 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.456 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.771 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.717 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.483 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.498 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.800 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.632 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.603 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.657 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.742 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.772 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.502 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.440 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.456 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.630 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.356 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.649 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.352 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.502 |
MOD_NEK2_2 | 88 | 93 | PF00069 | 0.365 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.734 |
MOD_PK_1 | 193 | 199 | PF00069 | 0.620 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.694 |
MOD_PKA_1 | 36 | 42 | PF00069 | 0.438 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.769 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.658 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.792 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.426 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.637 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.391 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.367 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.617 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.721 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.689 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.367 |
MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.582 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.749 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P923 | Leptomonas seymouri | 38% | 100% |
A0A3S5H659 | Leishmania donovani | 39% | 100% |
A0A3S7WQ87 | Leishmania donovani | 56% | 100% |
A4H5C7 | Leishmania braziliensis | 32% | 98% |
A4HTK6 | Leishmania infantum | 56% | 100% |
A4HTK7 | Leishmania infantum | 39% | 100% |
E9AMD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AMD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4QIB1 | Leishmania major | 36% | 100% |
Q4QIB2 | Leishmania major | 58% | 100% |