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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B0T9
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0042026 | protein refolding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0051082 | unfolded protein binding | 3 | 12 |
GO:0044183 | protein folding chaperone | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.582 |
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.530 |
CLV_MEL_PAP_1 | 280 | 286 | PF00089 | 0.300 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.339 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.524 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 142 | 148 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.279 |
DOC_MAPK_DCC_7 | 201 | 211 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 5 | 13 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 5 | 13 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.573 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.544 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.556 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 200 | 207 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 283 | 291 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 322 | 330 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 348 | 357 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 443 | 448 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.400 |
LIG_Actin_RPEL_3 | 35 | 54 | PF02755 | 0.429 |
LIG_deltaCOP1_diTrp_1 | 181 | 187 | PF00928 | 0.500 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.491 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.518 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.540 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.445 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.384 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.433 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 372 | 376 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 127 | 138 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 435 | 441 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.336 |
LIG_MAD2 | 121 | 129 | PF02301 | 0.480 |
LIG_NRBOX | 137 | 143 | PF00104 | 0.529 |
LIG_PCNA_yPIPBox_3 | 392 | 403 | PF02747 | 0.556 |
LIG_Pex14_1 | 183 | 187 | PF04695 | 0.491 |
LIG_REV1ctd_RIR_1 | 387 | 396 | PF16727 | 0.517 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 103 | 106 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.415 |
LIG_SH3_2 | 113 | 118 | PF14604 | 0.445 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.476 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.495 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.506 |
LIG_SUMO_SIM_par_1 | 328 | 334 | PF11976 | 0.448 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.470 |
LIG_WW_3 | 405 | 409 | PF00397 | 0.539 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.497 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.308 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.470 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.423 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.523 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.495 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.726 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.465 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.353 |
MOD_Cter_Amidation | 425 | 428 | PF01082 | 0.356 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.340 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.664 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.579 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.429 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.359 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.632 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.483 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.528 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.456 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.469 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.502 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.346 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.337 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.409 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.374 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.334 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.218 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.600 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.339 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.339 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.474 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.399 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.556 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.521 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.456 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.269 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.272 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.423 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.393 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.423 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.482 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.486 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.432 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.417 |
MOD_PKB_1 | 5 | 13 | PF00069 | 0.418 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.346 |
MOD_Plk_1 | 416 | 422 | PF00069 | 0.450 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.404 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.410 |
MOD_Plk_2-3 | 241 | 247 | PF00069 | 0.700 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.516 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.506 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.444 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.556 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.382 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.498 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.691 |
MOD_SUMO_rev_2 | 244 | 252 | PF00179 | 0.584 |
TRG_DiLeu_BaEn_1 | 293 | 298 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_4 | 81 | 87 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.258 |
TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 28 | 33 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAI4 | Leptomonas seymouri | 63% | 88% |
A0A0S4J763 | Bodo saltans | 24% | 100% |
A0A1X0P2N8 | Trypanosomatidae | 38% | 99% |
A0A3Q8IES4 | Leishmania donovani | 92% | 98% |
A0A422P4Y1 | Trypanosoma rangeli | 36% | 100% |
A4HIB0 | Leishmania braziliensis | 78% | 100% |
A4I5J4 | Leishmania infantum | 93% | 98% |
C9ZQT1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4Q7C7 | Leishmania major | 91% | 100% |
V5DQR0 | Trypanosoma cruzi | 34% | 100% |