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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4QH60
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.440 |
CLV_Separin_Metazoa | 77 | 81 | PF03568 | 0.462 |
DOC_MAPK_gen_1 | 142 | 151 | PF00069 | 0.467 |
DOC_MAPK_HePTP_8 | 141 | 153 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 144 | 153 | PF00069 | 0.473 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.651 |
LIG_Actin_WH2_2 | 38 | 54 | PF00022 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.681 |
LIG_CaM_IQ_9 | 134 | 149 | PF13499 | 0.405 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.665 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.612 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.434 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.517 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.600 |
LIG_PDZ_Class_2 | 179 | 184 | PF00595 | 0.525 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.560 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 75 | 80 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 28 | 33 | PF11976 | 0.490 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.449 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.650 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.401 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.628 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.571 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.479 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.662 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.544 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.609 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.710 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.432 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.681 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.608 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.547 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.712 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.590 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.606 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.597 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.475 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.695 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.525 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.599 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.724 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.489 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.525 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.639 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.648 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.629 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4P1 | Leptomonas seymouri | 44% | 100% |
A0A3R7M7U3 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WRH9 | Leishmania donovani | 89% | 100% |
A4H9T8 | Leishmania braziliensis | 75% | 80% |
A4HUT2 | Leishmania infantum | 89% | 100% |
E9ANG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |