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: A4HNI2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.427 |
DEG_SCF_FBW7_1 | 169 | 175 | PF00400 | 0.479 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.498 |
DOC_CKS1_1 | 216 | 221 | PF01111 | 0.468 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.469 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.450 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.527 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_EH_1 | 144 | 148 | PF12763 | 0.461 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.596 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.594 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 107 | 111 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 210 | 220 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.398 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.469 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.389 |
LIG_SH2_GRB2like | 108 | 111 | PF00017 | 0.573 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.625 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.514 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.497 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.644 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.639 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.580 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.776 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.590 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.475 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.445 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.464 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.419 |
LIG_WW_1 | 105 | 108 | PF00397 | 0.385 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.535 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.552 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.718 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.412 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.445 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.475 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.598 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.565 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.664 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.493 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.479 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.539 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.739 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.515 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.583 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.603 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.507 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.411 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.418 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.486 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.552 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.543 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.592 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.497 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.377 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.371 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.485 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.448 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.612 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.615 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.412 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.315 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.593 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.732 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.605 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.674 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.494 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.523 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL43 | Leptomonas seymouri | 56% | 90% |
A0A1X0P4Q8 | Trypanosomatidae | 46% | 100% |
A0A3S7XA28 | Leishmania donovani | 81% | 100% |
A4IC38 | Leishmania infantum | 81% | 100% |
E9AFZ3 | Leishmania major | 80% | 100% |
E9B746 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |