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: A4ICB2
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_NRD_NRD_1 | 169 | 171 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.623 |
CLV_PCSK_FUR_1 | 167 | 171 | PF00082 | 0.623 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.628 |
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 | 0.621 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.312 |
CLV_PCSK_PC7_1 | 314 | 320 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.524 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.593 |
DEG_SIAH_1 | 93 | 101 | PF03145 | 0.585 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.620 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.607 |
DOC_CYCLIN_yCln2_LP_2 | 292 | 298 | PF00134 | 0.657 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.602 |
DOC_MAPK_FxFP_2 | 36 | 39 | PF00069 | 0.554 |
DOC_MAPK_FxFP_2 | 6 | 9 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 288 | 296 | PF00069 | 0.614 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.352 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.653 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.554 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.537 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.586 |
LIG_CtBP_PxDLS_1 | 238 | 242 | PF00389 | 0.388 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.424 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.677 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.457 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 3 | 9 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 34 | 39 | PF02991 | 0.647 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.534 |
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 | 0.643 |
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 | 0.571 |
LIG_PCNA_yPIPBox_3 | 352 | 361 | PF02747 | 0.515 |
LIG_PCNA_yPIPBox_3 | 62 | 73 | PF02747 | 0.602 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.388 |
LIG_SH3_2 | 312 | 317 | PF14604 | 0.622 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.626 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.312 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.610 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.530 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.552 |
LIG_SUMO_SIM_anti_2 | 200 | 206 | PF11976 | 0.312 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.610 |
LIG_TRAF2_2 | 10 | 15 | PF00917 | 0.564 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.312 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.255 |
LIG_WW_2 | 123 | 126 | PF00397 | 0.617 |
MOD_CDC14_SPxK_1 | 30 | 33 | PF00782 | 0.616 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.612 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.653 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.543 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.576 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.613 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.342 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.598 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.642 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.568 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.345 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.674 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.618 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.653 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.312 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.626 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.718 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.600 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.676 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.678 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.312 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.539 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.640 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.565 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.770 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.574 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.639 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.312 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.535 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.597 |
MOD_Plk_2-3 | 240 | 246 | PF00069 | 0.255 |
MOD_Plk_2-3 | 351 | 357 | PF00069 | 0.509 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.570 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.473 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.663 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.600 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 210 | 217 | PF00179 | 0.276 |
MOD_SUMO_rev_2 | 326 | 336 | PF00179 | 0.694 |
TRG_DiLeu_BaEn_2 | 266 | 272 | PF01217 | 0.579 |
TRG_DiLeu_BaEn_4 | 267 | 273 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.317 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.680 |
TRG_NLS_Bipartite_1 | 251 | 265 | PF00514 | 0.478 |
TRG_NLS_MonoExtN_4 | 258 | 265 | PF00514 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZV5 | Leptomonas seymouri | 54% | 100% |
A0A3Q8IM42 | Leishmania donovani | 100% | 100% |
A4HQH6 | Leishmania braziliensis | 79% | 99% |
E9AU89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0A2 | Leishmania major | 92% | 100% |