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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AG88
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0000976 | transcription cis-regulatory region binding | 5 | 1 |
GO:0001067 | transcription regulatory region nucleic acid binding | 4 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 441 | 443 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.614 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.522 |
DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.532 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.443 |
DEG_SCF_FBW7_2 | 180 | 187 | PF00400 | 0.504 |
DEG_SCF_FBW7_2 | 252 | 259 | PF00400 | 0.710 |
DEG_SPOP_SBC_1 | 465 | 469 | PF00917 | 0.741 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.494 |
DOC_CKS1_1 | 181 | 186 | PF01111 | 0.510 |
DOC_CKS1_1 | 253 | 258 | PF01111 | 0.695 |
DOC_CYCLIN_RxL_1 | 218 | 225 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.488 |
DOC_MAPK_gen_1 | 27 | 35 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 316 | 327 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.480 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.639 |
DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.580 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.496 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.680 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 143 | 150 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 70 | 78 | PF00244 | 0.365 |
LIG_Actin_WH2_2 | 276 | 293 | PF00022 | 0.504 |
LIG_AP2alpha_2 | 147 | 149 | PF02296 | 0.554 |
LIG_APCC_ABBA_1 | 263 | 268 | PF00400 | 0.506 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.471 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.629 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.458 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.455 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.666 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.701 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.405 |
LIG_Integrin_RGD_1 | 459 | 461 | PF01839 | 0.745 |
LIG_LIR_Apic_2 | 55 | 60 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 410 | 417 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.588 |
LIG_PTAP_UEV_1 | 65 | 70 | PF05743 | 0.410 |
LIG_PTB_Apo_2 | 1 | 8 | PF02174 | 0.371 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 385 | 388 | PF00017 | 0.518 |
LIG_SH2_SRC | 266 | 269 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 192 | 196 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.321 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.585 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.547 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.639 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.622 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.394 |
LIG_SUMO_SIM_par_1 | 12 | 19 | PF11976 | 0.572 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.458 |
LIG_TRFH_1 | 109 | 113 | PF08558 | 0.475 |
LIG_TYR_ITIM | 411 | 416 | PF00017 | 0.676 |
LIG_UBA3_1 | 223 | 232 | PF00899 | 0.515 |
LIG_UBA3_1 | 83 | 91 | PF00899 | 0.412 |
MOD_CDK_SPK_2 | 501 | 506 | PF00069 | 0.657 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.427 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.630 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.429 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.550 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.635 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.601 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.762 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.673 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.405 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.627 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.641 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.691 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.699 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.597 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.537 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.614 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.512 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.496 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.716 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.556 |
MOD_N-GLC_2 | 138 | 140 | PF02516 | 0.476 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.586 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.574 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.573 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.737 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.578 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.599 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.498 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.581 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.589 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.412 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.466 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.626 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.511 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.639 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.503 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.454 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.714 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.495 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.505 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.552 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.593 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.588 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.485 |
MOD_SUMO_for_1 | 486 | 489 | PF00179 | 0.701 |
MOD_SUMO_rev_2 | 229 | 237 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_2 | 217 | 223 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.653 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.523 |
TRG_NLS_Bipartite_1 | 122 | 138 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWK4 | Leptomonas seymouri | 69% | 86% |
A0A1X0NGG7 | Trypanosomatidae | 40% | 93% |
A0A3S5H6A1 | Leishmania donovani | 100% | 88% |
A0A3S7WQF9 | Leishmania donovani | 100% | 100% |
A0A422NFU0 | Trypanosoma rangeli | 38% | 94% |
A4HC42 | Leishmania braziliensis | 86% | 100% |
C9ZPG2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 94% |
E9AMJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O94271 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 75% |
Q06436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 76% |
Q32NQ8 | Xenopus laevis | 23% | 67% |
Q4QI41 | Leishmania major | 97% | 100% |
V5DAD1 | Trypanosoma cruzi | 41% | 93% |