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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H788
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.561 |
CLV_PCSK_FUR_1 | 305 | 309 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.381 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.440 |
DEG_SCF_FBW7_1 | 160 | 166 | PF00400 | 0.571 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.592 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.562 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.752 |
DOC_CYCLIN_RxL_1 | 417 | 427 | PF00134 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 146 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 405 | 411 | PF00149 | 0.362 |
DOC_PP2B_LxvP_1 | 279 | 282 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 438 | 441 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.551 |
DOC_USP7_MATH_2 | 189 | 195 | PF00917 | 0.693 |
DOC_USP7_UBL2_3 | 180 | 184 | PF12436 | 0.693 |
DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 384 | 393 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.380 |
LIG_APCC_ABBAyCdc20_2 | 288 | 294 | PF00400 | 0.553 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.447 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.559 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.540 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.317 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.527 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.536 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.438 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.571 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.648 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 397 | 402 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.486 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.444 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.446 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.741 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.626 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.482 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.650 |
LIG_SH3_4 | 180 | 187 | PF00018 | 0.562 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 97 | 103 | PF11976 | 0.521 |
LIG_TRFH_1 | 426 | 430 | PF08558 | 0.495 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.463 |
MOD_CDC14_SPxK_1 | 302 | 305 | PF00782 | 0.555 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.550 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.676 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.574 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.566 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.700 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.704 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.438 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.571 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.548 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.519 |
MOD_Cter_Amidation | 315 | 318 | PF01082 | 0.561 |
MOD_DYRK1A_RPxSP_1 | 159 | 163 | PF00069 | 0.685 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.576 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.623 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.737 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.679 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.728 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.706 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.588 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.702 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.668 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.585 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.448 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.591 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.830 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.662 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.620 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.508 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.378 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.403 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.651 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.523 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.511 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.723 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.666 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.542 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.706 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.653 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.566 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.633 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.374 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.420 |
MOD_NEK2_2 | 253 | 258 | PF00069 | 0.565 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.307 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.396 |
MOD_PKA_1 | 184 | 190 | PF00069 | 0.562 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.669 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.393 |
MOD_PKB_1 | 128 | 136 | PF00069 | 0.438 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.423 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.564 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.487 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.565 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.370 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.373 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.567 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.557 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.722 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.676 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.712 |
MOD_SUMO_for_1 | 306 | 309 | PF00179 | 0.734 |
TRG_DiLeu_BaLyEn_6 | 101 | 106 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7S2 | Leptomonas seymouri | 45% | 100% |
A0A3S5H6P2 | Leishmania donovani | 72% | 100% |
A4HVM8 | Leishmania infantum | 72% | 100% |
E9APC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QG54 | Leishmania major | 71% | 100% |