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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0044183 | protein folding chaperone | 1 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
GO:0051087 | protein-folding chaperone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.594 |
CLV_MEL_PAP_1 | 2 | 8 | PF00089 | 0.472 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.529 |
CLV_PCSK_FUR_1 | 126 | 130 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.542 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.376 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.774 |
DOC_ANK_TNKS_1 | 140 | 147 | PF00023 | 0.512 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.480 |
DOC_PP1_SILK_1 | 199 | 204 | PF00149 | 0.616 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 4 | 13 | PF00244 | 0.402 |
LIG_AP2alpha_1 | 108 | 112 | PF02296 | 0.488 |
LIG_CaM_IQ_9 | 121 | 136 | PF13499 | 0.501 |
LIG_DLG_GKlike_1 | 289 | 297 | PF00625 | 0.572 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.575 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.502 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.494 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.459 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.648 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.507 |
LIG_Integrin_RGD_1 | 101 | 103 | PF01839 | 0.416 |
LIG_LIR_Apic_2 | 267 | 273 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 312 | 316 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.406 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.394 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.434 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.598 |
LIG_SH2_SRC | 270 | 273 | PF00017 | 0.656 |
LIG_SH2_SRC | 281 | 284 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.591 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.562 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.516 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.401 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.405 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.444 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.655 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.645 |
LIG_WRPW_2 | 226 | 229 | PF00400 | 0.423 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.530 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.588 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.430 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.725 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.610 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.574 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.642 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.450 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.488 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.366 |
MOD_DYRK1A_RPxSP_1 | 158 | 162 | PF00069 | 0.509 |
MOD_DYRK1A_RPxSP_1 | 55 | 59 | PF00069 | 0.711 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.463 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.533 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.764 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.756 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.754 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.583 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.536 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.516 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.571 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.770 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.773 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.732 |
MOD_LATS_1 | 204 | 210 | PF00433 | 0.441 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.527 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.638 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.540 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.650 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.507 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.378 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.540 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.691 |
MOD_PKB_1 | 71 | 79 | PF00069 | 0.526 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.627 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.509 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.712 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.542 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.479 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.663 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 110 | 117 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_4 | 167 | 173 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 17 | 20 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S6 | Leptomonas seymouri | 59% | 77% |
A0A0S4JEE6 | Bodo saltans | 30% | 99% |
A0A1X0P2B2 | Trypanosomatidae | 35% | 87% |
A0A3Q8IFJ9 | Leishmania donovani | 79% | 75% |
A0A3R7P4U9 | Trypanosoma rangeli | 36% | 94% |
A4I5D4 | Leishmania infantum | 79% | 100% |
C9ZQR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 82% |
E9B0N2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 74% |
Q4Q7K0 | Leishmania major | 78% | 100% |
V5BPN3 | Trypanosoma cruzi | 33% | 95% |