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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
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 |
Related structures:
AlphaFold database: A4HH91
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.430 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.570 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.527 |
DOC_CDC14_PxL_1 | 270 | 278 | PF14671 | 0.411 |
DOC_CDC14_PxL_1 | 340 | 348 | PF14671 | 0.501 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 381 | 391 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 211 | 219 | PF00069 | 0.388 |
DOC_MAPK_RevD_3 | 456 | 472 | PF00069 | 0.243 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.477 |
DOC_USP7_MATH_2 | 22 | 28 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.417 |
LIG_Actin_WH2_2 | 262 | 279 | PF00022 | 0.356 |
LIG_Actin_WH2_2 | 282 | 297 | PF00022 | 0.278 |
LIG_Actin_WH2_2 | 456 | 473 | PF00022 | 0.219 |
LIG_deltaCOP1_diTrp_1 | 296 | 306 | PF00928 | 0.437 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.477 |
LIG_Integrin_RGD_1 | 325 | 327 | PF01839 | 0.686 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.413 |
LIG_MYND_1 | 344 | 348 | PF01753 | 0.516 |
LIG_NRBOX | 454 | 460 | PF00104 | 0.374 |
LIG_PTB_Apo_2 | 450 | 457 | PF02174 | 0.247 |
LIG_SH2_PTP2 | 399 | 402 | PF00017 | 0.489 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.489 |
LIG_SH3_2 | 333 | 338 | PF14604 | 0.514 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.407 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.399 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.478 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.519 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.505 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.524 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.414 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.565 |
LIG_TRAF2_2 | 351 | 356 | PF00917 | 0.528 |
LIG_TYR_ITIM | 447 | 452 | PF00017 | 0.417 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.405 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.390 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.519 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.455 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.561 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.481 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.341 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.458 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.347 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.608 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.593 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.534 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.484 |
MOD_Cter_Amidation | 224 | 227 | PF01082 | 0.506 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.630 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.612 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.762 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.670 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.536 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.551 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.465 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.461 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.575 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.547 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.559 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.486 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.434 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.612 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.510 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.731 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.410 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.305 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.419 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.439 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.516 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.407 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.426 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.541 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.416 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.401 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.353 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.416 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.351 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.426 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.519 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.565 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.454 |
MOD_SUMO_rev_2 | 87 | 96 | PF00179 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q7 | Leptomonas seymouri | 59% | 95% |
A0A3S7X2C7 | Leishmania donovani | 72% | 99% |
A4I4D7 | Leishmania infantum | 72% | 99% |
C9ZL27 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 98% |
E9ADT6 | Leishmania major | 70% | 100% |
E9ALZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |