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 |
Related structures:
AlphaFold database: E9AZW0
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.644 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.772 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.716 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.574 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.579 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.578 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.628 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.660 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.315 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.754 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.612 |
DOC_PP4_MxPP_1 | 296 | 299 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 187 | 191 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 70 | 77 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.479 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.796 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.613 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.643 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.579 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.504 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.568 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.685 |
LIG_GSK3_LRP6_1 | 209 | 215 | PF00069 | 0.493 |
LIG_IBAR_NPY_1 | 370 | 372 | PF08397 | 0.679 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.315 |
LIG_LIR_Apic_2 | 172 | 177 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 59 | 66 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.611 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.686 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.515 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.459 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.570 |
LIG_SH3_1 | 391 | 397 | PF00018 | 0.488 |
LIG_SH3_2 | 386 | 391 | PF14604 | 0.683 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.584 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.628 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.508 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.564 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.469 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.612 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.633 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.724 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.611 |
MOD_CDC14_SPxK_1 | 375 | 378 | PF00782 | 0.522 |
MOD_CDC14_SPxK_1 | 388 | 391 | PF00782 | 0.682 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.618 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.689 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 385 | 391 | PF00069 | 0.680 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 142 | 149 | PF00069 | 0.579 |
MOD_CDK_SPxxK_3 | 169 | 176 | PF00069 | 0.599 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.501 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.650 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.665 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.702 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.653 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.709 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.621 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.590 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.680 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.661 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.629 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.619 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.679 |
MOD_DYRK1A_RPxSP_1 | 142 | 146 | PF00069 | 0.668 |
MOD_DYRK1A_RPxSP_1 | 149 | 153 | PF00069 | 0.513 |
MOD_DYRK1A_RPxSP_1 | 301 | 305 | PF00069 | 0.789 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.770 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.540 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.740 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.801 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.496 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.622 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.797 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.795 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.719 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.638 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.579 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.624 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.717 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.523 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.700 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.670 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.577 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.608 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.699 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.553 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.630 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.525 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.640 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.639 |
MOD_N-GLC_2 | 110 | 112 | PF02516 | 0.315 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.636 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.659 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.673 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.592 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.606 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.500 |
MOD_OFUCOSY | 120 | 126 | PF10250 | 0.315 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.555 |
MOD_PIKK_1 | 163 | 169 | PF00454 | 0.496 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.633 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.514 |
MOD_PK_1 | 362 | 368 | PF00069 | 0.509 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.347 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.608 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.721 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.514 |
MOD_PKB_1 | 142 | 150 | PF00069 | 0.609 |
MOD_PKB_1 | 257 | 265 | PF00069 | 0.464 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.612 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.592 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.613 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.583 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.720 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.569 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.606 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.493 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.558 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.641 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.775 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.535 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.630 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.787 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.618 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.627 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W6 | Leptomonas seymouri | 40% | 100% |
A0A3S7X1G7 | Leishmania donovani | 88% | 100% |
A4HGJ2 | Leishmania braziliensis | 64% | 100% |
E9ADK0 | Leishmania major | 87% | 100% |
E9AHG4 | Leishmania infantum | 88% | 100% |