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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: Q4Q465
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.628 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.538 |
DEG_COP1_1 | 219 | 227 | PF00400 | 0.577 |
DEG_SCF_FBW7_1 | 350 | 357 | PF00400 | 0.574 |
DEG_SPOP_SBC_1 | 181 | 185 | PF00917 | 0.568 |
DEG_SPOP_SBC_1 | 355 | 359 | PF00917 | 0.629 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.577 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.645 |
DOC_CYCLIN_yCln2_LP_2 | 214 | 220 | PF00134 | 0.674 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.646 |
DOC_PP2B_LxvP_1 | 214 | 217 | PF13499 | 0.672 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.548 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.517 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.559 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.602 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 63 | 67 | PF12436 | 0.794 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.560 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.634 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.659 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.645 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 2 | 8 | PF02991 | 0.618 |
LIG_LIR_Apic_2 | 298 | 304 | PF02991 | 0.625 |
LIG_LIR_Apic_2 | 56 | 62 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.560 |
LIG_MYND_1 | 279 | 283 | PF01753 | 0.524 |
LIG_MYND_1 | 304 | 308 | PF01753 | 0.621 |
LIG_Pex14_1 | 328 | 332 | PF04695 | 0.607 |
LIG_Pex14_1 | 379 | 383 | PF04695 | 0.572 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.524 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.587 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.552 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.784 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.668 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.654 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.472 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.572 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.569 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.619 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.513 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.511 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.603 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.662 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.674 |
LIG_TRFH_1 | 332 | 336 | PF08558 | 0.615 |
LIG_WW_3 | 202 | 206 | PF00397 | 0.646 |
MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.686 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.657 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.600 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.616 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.642 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.579 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.585 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.816 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.650 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.653 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.564 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.650 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.569 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.549 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.628 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.569 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.545 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.717 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.684 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.696 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.708 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.653 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.718 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.783 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.584 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.616 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.515 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.664 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.600 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.677 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.566 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.650 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.634 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.621 |
MOD_OFUCOSY | 141 | 146 | PF10250 | 0.567 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.596 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.811 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.574 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.601 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.555 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.554 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.631 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.630 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.576 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.631 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.647 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.625 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.616 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.633 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.540 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.659 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.677 |
MOD_SUMO_rev_2 | 327 | 337 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 69 | 78 | PF00179 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 276 | 281 | PF01217 | 0.519 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.554 |
TRG_NLS_MonoCore_2 | 312 | 317 | PF00514 | 0.627 |
TRG_NLS_MonoExtN_4 | 310 | 317 | PF00514 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITZ0 | Leishmania donovani | 89% | 71% |
A4I8Z0 | Leishmania infantum | 89% | 100% |
E9B3V9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |