RNA Processing, Splicing factor ptsr1-like
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HTB3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 301 | 305 | PF00082 | 0.735 |
CLV_PCSK_FUR_1 | 325 | 329 | PF00082 | 0.741 |
CLV_PCSK_FUR_1 | 338 | 342 | PF00082 | 0.501 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.722 |
CLV_PCSK_PC7_1 | 269 | 275 | PF00082 | 0.721 |
CLV_PCSK_PC7_1 | 293 | 299 | PF00082 | 0.697 |
CLV_PCSK_PC7_1 | 359 | 365 | PF00082 | 0.726 |
CLV_PCSK_PC7_1 | 367 | 373 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.559 |
DEG_APCC_KENBOX_2 | 159 | 163 | PF00400 | 0.619 |
DEG_SPOP_SBC_1 | 121 | 125 | PF00917 | 0.516 |
DOC_MAPK_gen_1 | 142 | 149 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.566 |
DOC_MAPK_RevD_3 | 248 | 261 | PF00069 | 0.501 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 311 | 317 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 88 | 93 | PF00244 | 0.563 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.717 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.529 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.553 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.545 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.459 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.522 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.602 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.494 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.705 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.548 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.551 |
LIG_GBD_Chelix_1 | 236 | 244 | PF00786 | 0.556 |
LIG_Integrin_RGD_1 | 367 | 369 | PF01839 | 0.650 |
LIG_NRP_CendR_1 | 372 | 375 | PF00754 | 0.698 |
LIG_PTB_Apo_2 | 135 | 142 | PF02174 | 0.545 |
LIG_PTB_Phospho_1 | 135 | 141 | PF10480 | 0.525 |
LIG_SH2_GRB2like | 180 | 183 | PF00017 | 0.603 |
LIG_SH2_NCK_1 | 224 | 228 | PF00017 | 0.375 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.592 |
LIG_SH3_2 | 69 | 74 | PF14604 | 0.720 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.610 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.735 |
LIG_SUMO_SIM_par_1 | 88 | 94 | PF11976 | 0.530 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.575 |
MOD_CDC14_SPxK_1 | 264 | 267 | PF00782 | 0.718 |
MOD_CDK_SPxK_1 | 261 | 267 | PF00069 | 0.717 |
MOD_CDK_SPxxK_3 | 304 | 311 | PF00069 | 0.738 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.592 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.733 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.753 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.676 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.571 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.492 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.562 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.589 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.536 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.648 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.565 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.631 |
MOD_Cter_Amidation | 325 | 328 | PF01082 | 0.743 |
MOD_DYRK1A_RPxSP_1 | 304 | 308 | PF00069 | 0.738 |
MOD_DYRK1A_RPxSP_1 | 328 | 332 | PF00069 | 0.736 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.606 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.555 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.534 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.630 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.719 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.739 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.588 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.511 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.586 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.527 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.736 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.632 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.503 |
MOD_LATS_1 | 285 | 291 | PF00433 | 0.733 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.749 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.518 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.656 |
MOD_PKA_1 | 287 | 293 | PF00069 | 0.736 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.732 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.740 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.675 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.750 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.544 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.669 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.754 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.509 |
MOD_PKB_1 | 287 | 295 | PF00069 | 0.735 |
MOD_PKB_1 | 319 | 327 | PF00069 | 0.742 |
MOD_PKB_1 | 352 | 360 | PF00069 | 0.556 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.529 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.530 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.546 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.562 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.752 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.735 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.789 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.717 |
TRG_DiLeu_BaEn_1 | 128 | 133 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.743 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.694 |
TRG_NLS_MonoCore_2 | 162 | 167 | PF00514 | 0.637 |
TRG_NLS_MonoExtC_3 | 162 | 168 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 160 | 167 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 130 | 135 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPZ1 | Leishmania donovani | 99% | 100% |
A4H537 | Leishmania braziliensis | 80% | 100% |
E9ALA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QIK0 | Leishmania major | 95% | 100% |