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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H7N5
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003743 | translation initiation factor activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.536 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.494 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 279 | 283 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 301 | 305 | PF00917 | 0.490 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.490 |
DOC_CDC14_PxL_1 | 188 | 196 | PF14671 | 0.667 |
DOC_CKS1_1 | 333 | 338 | PF01111 | 0.583 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.670 |
DOC_PP1_RVXF_1 | 148 | 155 | PF00149 | 0.490 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.655 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.663 |
DOC_USP7_MATH_2 | 236 | 242 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.569 |
DOC_USP7_UBL2_3 | 418 | 422 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.682 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 357 | 366 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.648 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.482 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.583 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.640 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.605 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.574 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.597 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.704 |
LIG_LIR_Apic_2 | 283 | 289 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.701 |
LIG_LIR_Apic_2 | 314 | 320 | PF02991 | 0.648 |
LIG_LIR_Apic_2 | 326 | 331 | PF02991 | 0.632 |
LIG_LIR_Apic_2 | 340 | 346 | PF02991 | 0.591 |
LIG_LIR_Apic_2 | 354 | 359 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.695 |
LIG_LIR_Apic_2 | 380 | 384 | PF02991 | 0.520 |
LIG_LIR_Apic_2 | 391 | 395 | PF02991 | 0.588 |
LIG_LIR_Apic_2 | 415 | 420 | PF02991 | 0.702 |
LIG_MYND_3 | 191 | 195 | PF01753 | 0.573 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.505 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.587 |
LIG_SH2_CRK | 309 | 313 | PF00017 | 0.558 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.628 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.623 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.704 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.635 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.636 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.525 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.686 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.691 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.623 |
LIG_SH2_PTP2 | 256 | 259 | PF00017 | 0.655 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.655 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.566 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.544 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.681 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.683 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.567 |
LIG_SH3_4 | 418 | 425 | PF00018 | 0.650 |
LIG_SUMO_SIM_par_1 | 78 | 83 | PF11976 | 0.489 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.671 |
LIG_TRAF2_1 | 193 | 196 | PF00917 | 0.616 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.587 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.669 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.683 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.767 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.650 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.714 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.602 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.663 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.679 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.715 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.561 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.501 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.511 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.536 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.738 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.774 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.572 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.667 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.709 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.575 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.709 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.782 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.649 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.488 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.770 |
MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.760 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.631 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.707 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.641 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.557 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.511 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.628 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.651 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.629 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.697 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.725 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.585 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.781 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.686 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.771 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.541 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.720 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.688 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.615 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.644 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.650 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.673 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.639 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.596 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.742 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.641 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.656 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.613 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.709 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.677 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.698 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.697 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.768 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.517 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.691 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.684 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.425 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.683 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.611 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.692 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.688 |
MOD_PK_1 | 393 | 399 | PF00069 | 0.488 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.686 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.485 |
MOD_PKA_1 | 202 | 208 | PF00069 | 0.688 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.441 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.746 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.688 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.641 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.674 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.648 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.577 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.665 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.661 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.681 |
MOD_SUMO_for_1 | 119 | 122 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 110 | 119 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 143 | 152 | PF00179 | 0.704 |
TRG_NLS_MonoExtC_3 | 19 | 25 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 17 | 24 | PF00514 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE22 | Leptomonas seymouri | 42% | 100% |
A0A1X0NNK6 | Trypanosomatidae | 32% | 89% |
A0A3R7RMH8 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WT08 | Leishmania donovani | 68% | 99% |
A4HW24 | Leishmania infantum | 68% | 99% |
C9ZT09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 84% |
E9APS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 96% |
Q4QFQ3 | Leishmania major | 68% | 97% |