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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4I430
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
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_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.579 |
CLV_PCSK_FUR_1 | 9 | 13 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.486 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.528 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.678 |
DOC_ANK_TNKS_1 | 12 | 19 | PF00023 | 0.728 |
DOC_CYCLIN_RxL_1 | 40 | 50 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.712 |
DOC_MAPK_gen_1 | 43 | 49 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.705 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.375 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.464 |
DOC_USP7_MATH_2 | 15 | 21 | PF00917 | 0.762 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 309 | 319 | PF00244 | 0.557 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.694 |
LIG_EVH1_2 | 276 | 280 | PF00568 | 0.685 |
LIG_EVH1_2 | 31 | 35 | PF00568 | 0.556 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.518 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.467 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.441 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.504 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.583 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.560 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.669 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.643 |
LIG_IBAR_NPY_1 | 323 | 325 | PF08397 | 0.552 |
LIG_LIR_Gen_1 | 191 | 202 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.570 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.508 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.433 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.712 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.706 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.398 |
LIG_UBA3_1 | 34 | 43 | PF00899 | 0.453 |
MOD_CDK_SPxxK_3 | 180 | 187 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.680 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.501 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.756 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.661 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.550 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.618 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.614 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.582 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.538 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.337 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.445 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.704 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.714 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.621 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.543 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.644 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.537 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.510 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.447 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.626 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.666 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.684 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.740 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.573 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.446 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.553 |
MOD_PKB_1 | 74 | 82 | PF00069 | 0.495 |
MOD_Plk_2-3 | 235 | 241 | PF00069 | 0.724 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.499 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.646 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.609 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.523 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.549 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.741 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.604 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.612 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 212 | 215 | PF00179 | 0.627 |
TRG_DiLeu_BaLyEn_6 | 119 | 124 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY30 | Leptomonas seymouri | 30% | 81% |
A0A0N1I3L5 | Leptomonas seymouri | 68% | 100% |
A0A1X0NQH6 | Trypanosomatidae | 41% | 100% |
A0A3R7R5S5 | Trypanosoma rangeli | 32% | 76% |
A0A3S5IR49 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X224 | Leishmania donovani | 99% | 100% |
A4HGZ8 | Leishmania braziliensis | 83% | 100% |
E9B0B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q7W7 | Leishmania major | 95% | 100% |
V5BI47 | Trypanosoma cruzi | 42% | 100% |