Histone/chromosome structure, TATA element modulatory factor 1 TATA binding
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HVH7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 14 | 20 | PF00089 | 0.662 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.662 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.626 |
CLV_Separin_Metazoa | 402 | 406 | PF03568 | 0.506 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.615 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.499 |
DOC_CDC14_PxL_1 | 370 | 378 | PF14671 | 0.744 |
DOC_MAPK_gen_1 | 311 | 317 | PF00069 | 0.597 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 123 | 132 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 173 | 177 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 207 | 213 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 369 | 374 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 405 | 413 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.617 |
LIG_Actin_WH2_2 | 128 | 146 | PF00022 | 0.607 |
LIG_Actin_WH2_2 | 158 | 175 | PF00022 | 0.618 |
LIG_Actin_WH2_2 | 310 | 327 | PF00022 | 0.625 |
LIG_APCC_Cbox_2 | 291 | 297 | PF00515 | 0.614 |
LIG_EH_1 | 376 | 380 | PF12763 | 0.746 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.586 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.600 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.700 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.571 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.619 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.476 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.589 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.574 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.661 |
LIG_GBD_Chelix_1 | 118 | 126 | PF00786 | 0.607 |
LIG_LIR_Gen_1 | 246 | 255 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 290 | 300 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.556 |
LIG_MYND_1 | 374 | 378 | PF01753 | 0.734 |
LIG_Pex14_1 | 289 | 293 | PF04695 | 0.609 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.612 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.566 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.505 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 147 | 150 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.617 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.681 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.615 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.614 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.510 |
LIG_UBA3_1 | 45 | 51 | PF00899 | 0.639 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.621 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.617 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.390 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.605 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.705 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.746 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.622 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.662 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.538 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.341 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.578 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.800 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.554 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.500 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.612 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.616 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.604 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.650 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.706 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.650 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.609 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.669 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.571 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.629 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.587 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.619 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.610 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.599 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.281 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.713 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.628 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.607 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.629 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.710 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.665 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.617 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.629 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.603 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.523 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.611 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.613 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.598 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.667 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.623 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.727 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.589 |
MOD_NEK2_2 | 378 | 383 | PF00069 | 0.620 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.608 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.611 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.565 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.801 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.610 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.617 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.545 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.562 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.568 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.610 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.642 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.454 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.634 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.540 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.681 |
MOD_Plk_2-3 | 221 | 227 | PF00069 | 0.617 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.560 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.592 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.608 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.661 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 141 | 146 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 389 | 395 | PF00179 | 0.689 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_1 | 432 | 437 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_4 | 61 | 67 | PF01217 | 0.638 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 292 | 297 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.471 |
TRG_PTS2 | 1 | 25 | PF00400 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3R7L520 | Trypanosoma rangeli | 27% | 70% |
D0A6T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 74% |
E9AP72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 68% |
Q4QGA6 | Leishmania major | 94% | 100% |