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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A0A3S7WWZ1
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
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 | 202 | 206 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.317 |
DEG_Kelch_Keap1_1 | 191 | 196 | PF01344 | 0.607 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.383 |
DOC_MAPK_MEF2A_6 | 215 | 222 | PF00069 | 0.426 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.352 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.436 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.507 |
DOC_USP7_MATH_2 | 168 | 174 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 292 | 300 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.676 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.618 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.475 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.562 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.325 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.616 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.685 |
LIG_IBAR_NPY_1 | 400 | 402 | PF08397 | 0.515 |
LIG_LIR_Apic_2 | 137 | 142 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 302 | 306 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 264 | 275 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.283 |
LIG_MYND_1 | 376 | 380 | PF01753 | 0.572 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.597 |
LIG_SH2_SRC | 402 | 405 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.535 |
LIG_UBA3_1 | 241 | 249 | PF00899 | 0.399 |
LIG_WW_3 | 166 | 170 | PF00397 | 0.535 |
MOD_CDK_SPxK_1 | 286 | 292 | PF00069 | 0.553 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.523 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.704 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.568 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.587 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.746 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.552 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.614 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.387 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.619 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.410 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.523 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.728 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.678 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.606 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.562 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.564 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.488 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.541 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.640 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.624 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.409 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.493 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.630 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.668 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.559 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.639 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.690 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.608 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.712 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.609 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.413 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.582 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.709 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.577 |
MOD_N-GLC_2 | 224 | 226 | PF02516 | 0.439 |
MOD_N-GLC_2 | 263 | 265 | PF02516 | 0.341 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.513 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.477 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.753 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.710 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.666 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.720 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.524 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.628 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.609 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.540 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.478 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.625 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.680 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.615 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.424 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.604 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.483 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.393 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.713 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.712 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.633 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.502 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.397 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.587 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.546 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_1 | 98 | 103 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_3 | 236 | 242 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 54 | 59 | PF01217 | 0.508 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.622 |
TRG_ER_FFAT_2 | 304 | 315 | PF00635 | 0.474 |
TRG_NES_CRM1_1 | 100 | 112 | PF08389 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY30 | Leptomonas seymouri | 59% | 99% |
A0A1X0NUJ7 | Trypanosomatidae | 36% | 100% |
A0A3R7MUT8 | Trypanosoma rangeli | 36% | 100% |
A4HC69 | Leishmania braziliensis | 73% | 100% |
A4HZP4 | Leishmania infantum | 100% | 100% |
E9AVK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QBX9 | Leishmania major | 94% | 100% |
V5DBU7 | Trypanosoma cruzi | 37% | 100% |