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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QCZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003839 | gamma-glutamylcyclotransferase activity | 5 | 7 |
GO:0016829 | lyase activity | 2 | 7 |
GO:0016840 | carbon-nitrogen lyase activity | 3 | 7 |
GO:0016842 | amidine-lyase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.328 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.371 |
DOC_MAPK_gen_1 | 246 | 256 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 332 | 343 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 249 | 256 | PF00069 | 0.585 |
DOC_MAPK_NFAT4_5 | 249 | 257 | PF00069 | 0.536 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.430 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.424 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.573 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.704 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.493 |
LIG_CtBP_PxDLS_1 | 70 | 74 | PF00389 | 0.474 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.336 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.260 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.596 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.382 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.351 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.413 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.384 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.309 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.567 |
LIG_GBD_Chelix_1 | 107 | 115 | PF00786 | 0.312 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.651 |
LIG_LIR_Gen_1 | 250 | 258 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 318 | 326 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 428 | 434 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.461 |
LIG_MYND_1 | 43 | 47 | PF01753 | 0.452 |
LIG_PCNA_yPIPBox_3 | 187 | 201 | PF02747 | 0.556 |
LIG_Pex14_1 | 309 | 313 | PF04695 | 0.354 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.464 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.377 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.528 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.460 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 359 | 362 | PF00017 | 0.446 |
LIG_SH2_PTP2 | 340 | 343 | PF00017 | 0.351 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.378 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.360 |
LIG_SH2_STAT3 | 432 | 435 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.416 |
LIG_SH3_1 | 467 | 473 | PF00018 | 0.401 |
LIG_SH3_2 | 470 | 475 | PF14604 | 0.473 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.510 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.619 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.596 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.475 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.489 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.451 |
LIG_WW_1 | 459 | 462 | PF00397 | 0.294 |
MOD_CDC14_SPxK_1 | 84 | 87 | PF00782 | 0.655 |
MOD_CDK_SPK_2 | 473 | 478 | PF00069 | 0.544 |
MOD_CDK_SPxK_1 | 81 | 87 | PF00069 | 0.650 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.465 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.663 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.565 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.458 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.488 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.384 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.412 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.345 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.591 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.569 |
MOD_GlcNHglycan | 110 | 114 | PF01048 | 0.422 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.690 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.497 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.503 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.346 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.404 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.741 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.670 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.389 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.422 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.617 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.478 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.680 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.296 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.450 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.421 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.507 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.636 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.507 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.571 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.577 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.395 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.345 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.458 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.420 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.344 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.447 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.411 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.394 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.296 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.456 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.597 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.582 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.493 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.707 |
MOD_SUMO_rev_2 | 300 | 308 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 90 | 99 | PF00179 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 447 | 450 | PF00400 | 0.245 |
TRG_NES_CRM1_1 | 153 | 169 | PF08389 | 0.380 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P468 | Leptomonas seymouri | 55% | 96% |
A0A3Q8IAR7 | Leishmania donovani | 90% | 100% |
A4HYM3 | Leishmania infantum | 90% | 100% |
E9AIA3 | Leishmania braziliensis | 74% | 99% |
E9AUI8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |