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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AWY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 13 |
GO:0006476 | protein deacetylation | 6 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0016570 | histone modification | 5 | 13 |
GO:0016575 | histone deacetylation | 6 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0035601 | protein deacylation | 5 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0098732 | macromolecule deacylation | 5 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004407 | histone deacetylase activity | 4 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 13 |
GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 13 |
GO:0019213 | deacetylase activity | 3 | 13 |
GO:0033558 | protein lysine deacetylase activity | 3 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:0005488 | binding | 1 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.436 |
CLV_PCSK_FUR_1 | 486 | 490 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.694 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.470 |
DEG_SCF_TRCP1_1 | 504 | 510 | PF00400 | 0.428 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.550 |
DOC_ANK_TNKS_1 | 502 | 509 | PF00023 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 432 | 440 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 254 | 262 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 432 | 440 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 460 | 467 | PF00149 | 0.284 |
DOC_PP1_RVXF_1 | 82 | 89 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.441 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 439 | 442 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 133 | 140 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 277 | 282 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 326 | 336 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.615 |
LIG_APCC_ABBA_1 | 436 | 441 | PF00400 | 0.375 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.739 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_2 | 166 | 172 | PF00533 | 0.512 |
LIG_CaM_IQ_9 | 461 | 477 | PF13499 | 0.442 |
LIG_eIF4E_1 | 98 | 104 | PF01652 | 0.473 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.486 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.480 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.403 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.353 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.530 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.493 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.648 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.470 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.747 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.693 |
LIG_GBD_Chelix_1 | 241 | 249 | PF00786 | 0.286 |
LIG_GBD_Chelix_1 | 350 | 358 | PF00786 | 0.245 |
LIG_Integrin_RGD_1 | 211 | 213 | PF01839 | 0.312 |
LIG_LIR_Apic_2 | 173 | 177 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 123 | 134 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.333 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.501 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.368 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.486 |
LIG_PTB_Apo_2 | 285 | 292 | PF02174 | 0.445 |
LIG_Rb_LxCxE_1 | 202 | 215 | PF01857 | 0.445 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.393 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 257 | 260 | PF00017 | 0.544 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.316 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.445 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.449 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.394 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.403 |
LIG_SUMO_SIM_par_1 | 371 | 376 | PF11976 | 0.440 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.434 |
LIG_TRAF2_1 | 497 | 500 | PF00917 | 0.478 |
LIG_TRAF2_1 | 540 | 543 | PF00917 | 0.448 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.622 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.486 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.468 |
MOD_CDK_SPK_2 | 427 | 432 | PF00069 | 0.442 |
MOD_CDK_SPK_2 | 44 | 49 | PF00069 | 0.604 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.439 |
MOD_CDK_SPxxK_3 | 64 | 71 | PF00069 | 0.544 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.695 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.667 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.542 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.736 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.716 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.662 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.435 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.693 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.565 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.660 |
MOD_Cter_Amidation | 80 | 83 | PF01082 | 0.463 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.790 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.266 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.240 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.569 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.276 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.614 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.619 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.562 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.766 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.666 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.607 |
MOD_GlcNHglycan | 61 | 65 | PF01048 | 0.669 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.555 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.490 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.512 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.697 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.674 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.698 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.615 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.711 |
MOD_LATS_1 | 131 | 137 | PF00433 | 0.512 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.589 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.428 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.453 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.479 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.486 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.486 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.541 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.406 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.300 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.408 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.468 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.573 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.353 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.501 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.475 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.493 |
MOD_PKA_1 | 432 | 438 | PF00069 | 0.396 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.445 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.512 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.468 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.364 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.550 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.514 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.515 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.468 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.673 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.394 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.440 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.526 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.445 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.690 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.678 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.599 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.694 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.590 |
MOD_SUMO_rev_2 | 67 | 73 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 486 | 489 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 254 | 259 | PF00026 | 0.286 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCD3 | Leptomonas seymouri | 80% | 100% |
A0A1X0NVQ2 | Trypanosomatidae | 72% | 100% |
A0A3Q8IC47 | Leishmania donovani | 95% | 100% |
A0A3S7WWE6 | Leishmania donovani | 39% | 100% |
A0A422N1V5 | Trypanosoma rangeli | 71% | 100% |
A4HBR4 | Leishmania braziliensis | 38% | 100% |
A4HDK5 | Leishmania braziliensis | 94% | 100% |
A4HZ67 | Leishmania infantum | 39% | 100% |
A4I0X6 | Leishmania infantum | 95% | 100% |
E9AV34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
O15379 | Homo sapiens | 36% | 100% |
O88895 | Mus musculus | 37% | 100% |
P56520 | Gallus gallus | 37% | 100% |
P64375 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 28% | 100% |
P64376 | Staphylococcus aureus (strain N315) | 28% | 100% |
Q28DV3 | Xenopus tropicalis | 37% | 100% |
Q4QAJ4 | Leishmania major | 94% | 100% |
Q4QCE7 | Leishmania major | 39% | 100% |
Q4SFA0 | Tetraodon nigroviridis | 36% | 100% |
Q5HF39 | Staphylococcus aureus (strain COL) | 28% | 100% |
Q5RB76 | Pongo abelii | 36% | 100% |
Q6G8J2 | Staphylococcus aureus (strain MSSA476) | 28% | 100% |
Q6GFX3 | Staphylococcus aureus (strain MRSA252) | 28% | 100% |
Q6IRL9 | Xenopus laevis | 37% | 100% |
Q6P6W3 | Rattus norvegicus | 37% | 100% |
Q7SXM0 | Danio rerio | 39% | 100% |
Q803C3 | Danio rerio | 36% | 100% |
Q8NW34 | Staphylococcus aureus (strain MW2) | 28% | 100% |