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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000126 | transcription factor TFIIIB complex | 4 | 1 |
GO:0005667 | transcription regulator complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0090576 | RNA polymerase III transcription regulator complex | 3 | 1 |
Related structures:
AlphaFold database: A4HQH6
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065004 | protein-DNA complex assembly | 6 | 1 |
GO:0070897 | transcription preinitiation complex assembly | 7 | 1 |
GO:0070898 | RNA polymerase III preinitiation complex assembly | 8 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001025 | RNA polymerase III general transcription initiation factor binding | 5 | 1 |
GO:0001156 | TFIIIC-class transcription factor complex binding | 6 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008134 | transcription factor binding | 3 | 1 |
GO:0140296 | general transcription initiation factor binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.662 |
CLV_PCSK_FUR_1 | 167 | 171 | PF00082 | 0.639 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.660 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.312 |
CLV_PCSK_PC7_1 | 314 | 320 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.524 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.613 |
DEG_SIAH_1 | 93 | 101 | PF03145 | 0.609 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 292 | 298 | PF00134 | 0.681 |
DOC_MAPK_FxFP_2 | 36 | 39 | PF00069 | 0.550 |
DOC_MAPK_FxFP_2 | 6 | 9 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.352 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.679 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.611 |
LIG_APCC_ABBA_1 | 358 | 363 | PF00400 | 0.399 |
LIG_CtBP_PxDLS_1 | 238 | 242 | PF00389 | 0.388 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.446 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.553 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.255 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.641 |
LIG_LIR_Apic_2 | 3 | 9 | PF02991 | 0.578 |
LIG_LIR_Apic_2 | 34 | 39 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 187 | 195 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 197 | 207 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 353 | 360 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.542 |
LIG_PCNA_yPIPBox_3 | 352 | 362 | PF02747 | 0.484 |
LIG_PCNA_yPIPBox_3 | 62 | 73 | PF02747 | 0.588 |
LIG_PDZ_Class_2 | 389 | 394 | PF00595 | 0.495 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.388 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.596 |
LIG_SH3_2 | 312 | 317 | PF14604 | 0.660 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.559 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.312 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.566 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.543 |
LIG_SUMO_SIM_anti_2 | 200 | 206 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 369 | 374 | PF11976 | 0.428 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.628 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.553 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.312 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.674 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.710 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.638 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.342 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.669 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.345 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.731 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.591 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.630 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.606 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.645 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.312 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.574 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.582 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.467 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.478 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.684 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.434 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.695 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.312 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.231 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.466 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.667 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.470 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.797 |
MOD_PKB_1 | 167 | 175 | PF00069 | 0.471 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.312 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.579 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.421 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.551 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.473 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.675 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.595 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 326 | 336 | PF00179 | 0.716 |
MOD_SUMO_rev_2 | 363 | 369 | PF00179 | 0.408 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_2 | 266 | 272 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_4 | 267 | 273 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.713 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZV5 | Leptomonas seymouri | 49% | 100% |
A0A3Q8IM42 | Leishmania donovani | 79% | 99% |
A4ICB2 | Leishmania infantum | 79% | 99% |
E9AU89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4Q0A2 | Leishmania major | 80% | 100% |