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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4ICK5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.551 |
CLV_MEL_PAP_1 | 145 | 151 | PF00089 | 0.577 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.439 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.596 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.409 |
DOC_CYCLIN_RxL_1 | 190 | 199 | PF00134 | 0.613 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 14 | 21 | PF00134 | 0.447 |
DOC_MAPK_MEF2A_6 | 14 | 21 | PF00069 | 0.337 |
DOC_MIT_MIM_1 | 179 | 191 | PF04212 | 0.503 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.335 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.678 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 148 | 155 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 208 | 214 | PF00244 | 0.616 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.344 |
LIG_APCC_ABBA_1 | 64 | 69 | PF00400 | 0.355 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.538 |
LIG_Integrin_isoDGR_2 | 133 | 135 | PF01839 | 0.546 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.335 |
LIG_Rb_LxCxE_1 | 214 | 231 | PF01857 | 0.518 |
LIG_Rb_LxCxE_1 | 23 | 45 | PF01857 | 0.305 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.523 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.335 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 86 | 90 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.355 |
LIG_SH3_2 | 109 | 114 | PF14604 | 0.603 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.354 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.432 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.338 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.473 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.383 |
LIG_WW_3 | 107 | 111 | PF00397 | 0.508 |
MOD_CDC14_SPxK_1 | 166 | 169 | PF00782 | 0.568 |
MOD_CDK_SPxK_1 | 163 | 169 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 135 | 142 | PF00069 | 0.666 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.699 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.710 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.597 |
MOD_DYRK1A_RPxSP_1 | 135 | 139 | PF00069 | 0.566 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.671 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.734 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.688 |
MOD_GlcNHglycan | 44 | 48 | PF01048 | 0.423 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.587 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.651 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.621 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.414 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.447 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.728 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.487 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.585 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.600 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.447 |
MOD_PKA_1 | 209 | 215 | PF00069 | 0.617 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.754 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.432 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.676 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.617 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.480 |
MOD_PKB_1 | 114 | 122 | PF00069 | 0.745 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.438 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.624 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.659 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.739 |
TRG_DiLeu_BaEn_1 | 214 | 219 | PF01217 | 0.567 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.614 |
TRG_DiLeu_BaEn_3 | 238 | 244 | PF01217 | 0.561 |
TRG_DiLeu_LyEn_5 | 214 | 219 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2R9 | Leptomonas seymouri | 50% | 93% |
A0A0S4J2G2 | Bodo saltans | 41% | 100% |
A0A1X0P9F2 | Trypanosomatidae | 44% | 100% |
A0A3Q8IH20 | Leishmania donovani | 100% | 100% |
A0A422N0I0 | Trypanosoma rangeli | 44% | 100% |
A4HNY8 | Leishmania braziliensis | 76% | 100% |
E9ASQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1U5 | Leishmania major | 90% | 100% |
V5BQB2 | Trypanosoma cruzi | 40% | 100% |