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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF26
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.503 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.552 |
CLV_Separin_Metazoa | 136 | 140 | PF03568 | 0.461 |
DEG_APCC_DBOX_1 | 298 | 306 | PF00400 | 0.636 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.647 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 191 | PF00134 | 0.361 |
DOC_MAPK_MEF2A_6 | 30 | 38 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.512 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.514 |
DOC_USP7_MATH_2 | 387 | 393 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 330 | 339 | PF00244 | 0.446 |
LIG_AP2alpha_2 | 204 | 206 | PF02296 | 0.483 |
LIG_BIR_III_4 | 221 | 225 | PF00653 | 0.627 |
LIG_eIF4E_1 | 152 | 158 | PF01652 | 0.514 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.382 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.417 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.288 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.453 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.386 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.381 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.653 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.533 |
LIG_LIR_Apic_2 | 201 | 205 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 411 | 415 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.568 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.489 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.398 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.398 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.566 |
LIG_SH3_2 | 286 | 291 | PF14604 | 0.462 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 79 | 86 | PF11976 | 0.325 |
LIG_TRAF2_2 | 216 | 221 | PF00917 | 0.578 |
LIG_WW_3 | 90 | 94 | PF00397 | 0.552 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.694 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.651 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.393 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.571 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.567 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.617 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.547 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.716 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.442 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.371 |
MOD_GlcNHglycan | 293 | 297 | PF01048 | 0.625 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.704 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.383 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.711 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.717 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.442 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.442 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.644 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.533 |
MOD_N-GLC_2 | 62 | 64 | PF02516 | 0.363 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.577 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.650 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.439 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.518 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.386 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.649 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.396 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.619 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.493 |
MOD_PKB_1 | 299 | 307 | PF00069 | 0.473 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.511 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.465 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.472 |
MOD_Plk_2-3 | 335 | 341 | PF00069 | 0.540 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.726 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.364 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.357 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.495 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.406 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.509 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.671 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.586 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.622 |
MOD_SUMO_rev_2 | 392 | 400 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 120 | 125 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.702 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBW3 | Leptomonas seymouri | 59% | 97% |
A0A0S4IN38 | Bodo saltans | 33% | 100% |
A0A1X0NQK8 | Trypanosomatidae | 44% | 100% |
A0A3R7KDQ9 | Trypanosoma rangeli | 45% | 100% |
A4HGW3 | Leishmania braziliensis | 82% | 99% |
A4I3Z3 | Leishmania infantum | 100% | 100% |
D0A963 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B083 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q802 | Leishmania major | 92% | 100% |
V5BC55 | Trypanosoma cruzi | 44% | 100% |