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: A4HHC9
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.821 |
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.539 |
CLV_MEL_PAP_1 | 142 | 148 | PF00089 | 0.715 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.655 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.755 |
DEG_SCF_TRCP1_1 | 183 | 188 | PF00400 | 0.581 |
DEG_SPOP_SBC_1 | 171 | 175 | PF00917 | 0.634 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.469 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.661 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.739 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.530 |
DOC_USP7_MATH_2 | 107 | 113 | PF00917 | 0.558 |
DOC_USP7_MATH_2 | 47 | 53 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 14 | 24 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 162 | 171 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.494 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.810 |
LIG_CaM_IQ_9 | 51 | 67 | PF13499 | 0.646 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.599 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.502 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.561 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.685 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.437 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.557 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.479 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.787 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.586 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 302 | 309 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 335 | 345 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 40 | 48 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.769 |
LIG_PALB2_WD40_1 | 299 | 307 | PF16756 | 0.501 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.530 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.739 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.531 |
LIG_SH3_2 | 244 | 249 | PF14604 | 0.717 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.570 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.655 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.663 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.531 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.614 |
LIG_Sin3_3 | 359 | 366 | PF02671 | 0.355 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.587 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.560 |
LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.639 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.257 |
LIG_UBA3_1 | 23 | 32 | PF00899 | 0.535 |
MOD_CDK_SPK_2 | 80 | 85 | PF00069 | 0.482 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.671 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.663 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.557 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.706 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.781 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.650 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.256 |
MOD_Cter_Amidation | 160 | 163 | PF01082 | 0.457 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.689 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.618 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.553 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.715 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.665 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.668 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.812 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.723 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.818 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.763 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.609 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.636 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.477 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.778 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.623 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.553 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.527 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.530 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.439 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.744 |
MOD_NEK2_2 | 252 | 257 | PF00069 | 0.378 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.488 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.667 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.777 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.756 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.506 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.698 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.616 |
MOD_Plk_2-3 | 210 | 216 | PF00069 | 0.567 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.606 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.640 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.697 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.547 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.459 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.394 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.584 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.570 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.593 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.679 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.522 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.505 |
MOD_SUMO_rev_2 | 103 | 112 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_2 | 48 | 54 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.621 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 99 | 103 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W0 | Leptomonas seymouri | 48% | 100% |
A0A3Q8IRA6 | Leishmania donovani | 73% | 99% |
A4I4H4 | Leishmania infantum | 72% | 99% |
E9ADX5 | Leishmania major | 71% | 100% |
E9ALV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |